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  • Read: Rescuing a Complex Hematology Oncology Trial: Case Study in Precision Rescuing a Complex Hematology Oncology Trial: Case Study in Precision

    Clinical Trials

    Rescuing a Complex Hematology Oncology Trial: Case Study in Precision

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      has third author: false, (SizeLimitingPyMap: {main={hs_id=164713188766, hs_child_table_id=0, hs_updated_at=1714747844927, hs_published_at=1738849393727, description=Anne Kopko is a Clinical Science Analytics & Insights Principal Scientist with fifteen years of professional oncology clinical research experience supporting Phase 1-3 clinical trials across a variety of therapeutic areas, including first-in-human, Phase 1-2 combination trials, dose escalation and expansion hematology and solid tumor studies. She plays a pivotal role in navigating the complex landscape of clinical data quality and supporting the cross-functional data cleaning process. She is a knowledgeable and collaborative partner with a passion to deliver quality data to her clients through a holistic, clinical sense data review approach., avatar=Image{width=300,height=300,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/Anne-Kopko-300x300.jpeg',altText='Anne-Kopko-300x300',fileId=164721973774}, linkedin=https://www.linkedin.com/in/anne-kopko-39b16888/, lastname=Kopko, hs_initial_published_at=1713363230550, hs_created_by_user_id=5166971, hs_created_at=1713362764236, hs_is_edited=false, hs_deleted_at=0, name=Anne, job=Manager, Clinical Oncology Solutions, slug=anne-kopko, hs_updated_by_user_id=26433386}, second={hs_id=182260357962, hs_child_table_id=0, hs_updated_at=1730486118009, hs_published_at=1738849393727, description=Andrea Chavlovich is Senior Clinical Scientist and contact for Clinical Science Analytics & Insights (CSAI). She is a hematology/oncology nurse (BSN, RN, BS) with over seven years of clinical research experience, both at the CRO and site levels. Andrea has worked on Phase 1-4 Oncology studies, including First-In-Human (FIH), Dose Escalation, and Dose Expansion. She has experience in hematology, cellular therapy, solid tumor, and rare disease studies, including but not limited to AML, breast cancer, and pancreatic malignancies. ​, avatar=Image{width=250,height=248,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Andrea%20Chavlovich%E2%80%8B.jpg',altText='Andrea Chavlovich​',fileId=182263330445}, lastname=Chavlovich​, hs_initial_published_at=1730486124094, hs_created_by_user_id=26433386, hs_created_at=1730485944077, hs_is_edited=false, hs_deleted_at=0, name=Andrea​, job=Senior Clinical Scientist, slug=andrea-chavlovich​, hs_updated_by_user_id=26433386}, third={hs_id=164713188782, hs_child_table_id=0, hs_updated_at=1714747852941, hs_published_at=1738849393727, description=Hasni M’hidi, PhD is a seasoned oncology clinical research professional, passionate about advancing medical science. As Global Project Manager, Hasni oversees operations in the US and EU. His expertise spans all phases of clinical trials, and his commitment to improving patient outcomes is unwavering., avatar=Image{width=300,height=300,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/Hasni-Mhidi-300x300.jpeg',altText='Hasni-Mhidi-300x300',fileId=164721971514}, linkedin=https://www.linkedin.com/in/hasni-m-hidi-4902b086/, lastname=M’hidi, PhD, hs_initial_published_at=1713363230550, hs_created_by_user_id=5166971, hs_created_at=1713362890341, hs_is_edited=false, hs_deleted_at=0, name=Hasni, job=Project Manager, slug=hasni-mhidi, hs_updated_by_user_id=26433386}})
    • Anne K. avatar Andrea​ C. avatar Hasni M. avatar
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      Hasni M.

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  • Read: Safety isn’t a Milestone but a Mindset in Clinical Research Safety isn’t a Milestone but a Mindset in Clinical Research

    Clinical Trials

    Safety isn’t a Milestone but a Mindset in Clinical Research

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=178509987401, hs_child_table_id=0, hs_updated_at=1726513291967, hs_published_at=1738849393727, description=Renise Blythe brings over 20 years of extensive experience in pharmacovigilance, drug safety, regulatory affairs, and risk management. She brings a wealth of knowledge and a proven track record of success in oncology, critical care, and women’s health., avatar=Image{width=513,height=640,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Renise%20Blythe.jpg',altText='Renise Blythe',fileId=178541750861}, lastname=Blythe, hs_initial_published_at=1726512636738, hs_created_by_user_id=26433386, hs_created_at=1726499253453, hs_is_edited=false, hs_deleted_at=0, name=Renise, job=Vice President, Global Drug Safety, slug=renise-blythe, hs_updated_by_user_id=51739740}, second={}, third={}})
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      Renise Blythe

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  • Read: Case Study: Streamlining Radiopharmaceutical Clinical Trials Case Study: Streamlining Radiopharmaceutical Clinical Trials

    Oncology

    Case Study: Streamlining Radiopharmaceutical Clinical Trials

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=169565849889, hs_child_table_id=0, hs_updated_at=1723217264651, hs_published_at=1738849393727, avatar=Image{width=320,height=314,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Tai%20Bibbs.jpg',altText='Tai Bibbs',fileId=168843139243}, lastname=Bibbs, hs_initial_published_at=1718988967067, hs_created_by_user_id=26433386, hs_created_at=1717603645564, hs_is_edited=false, hs_deleted_at=0, name=Tai, job=Director, Project Management, slug=tai-bibbs, hs_updated_by_user_id=26433386}, second={}, third={}})
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      Tai Bibbs

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  • Read: Navigating Site Activation Strategy Under the EU Clinical Trials Regulation Navigating Site Activation Strategy Under the EU Clinical Trials Regulation

    Regulatory

    Navigating Site Activation Strategy Under the EU Clinical Trials Regulation

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=169565849890, hs_child_table_id=0, hs_updated_at=1723217327146, hs_published_at=1738849393727, avatar=Image{width=800,height=800,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Barbara%20Kathage.jpg',altText='Barbara Kathage',fileId=168426405902}, lastname=Kathage, hs_initial_published_at=1718988967067, hs_created_by_user_id=26433386, hs_created_at=1717603865843, hs_is_edited=false, hs_deleted_at=0, name=Barbara, job=Vice President, Site Start Up, slug=barbara-kathage, hs_updated_by_user_id=26433386}, second={hs_id=159488778852, hs_child_table_id=0, hs_updated_at=1716212815818, hs_published_at=1738849393727, description=Chris Ingram, BSc (Hons) is Head of Regulatory Consultancy (Europe) for Precision for Medicine. Chris received his BSc(Hons) in immunology and pharmacology from the University of Strathclyde and has since spent over 21 years working in regulatory affairs with a focus on clinical development. Chris’ regulatory expertise covers clinical development across all phases, regulatory strategy, marketing authorisations, scientific advice, orphan drug designation and paediatric investigation plans across a wide variety of therapeutic areas, including but not limited to, oncology, CNS, metabolic, endocrinology, analgesia and cardiovascular., avatar=Image{width=576,height=576,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Chris%20Ingram.webp',altText='Chris Ingram',fileId=165893120791}, linkedin=https://www.linkedin.com/in/chris-ingram-0255b216, hs_name=, hs_path=, lastname=Ingram, hs_initial_published_at=1716212950453, hs_created_at=1709645745083, hs_is_edited=false, hs_deleted_at=0, name=Chris, job=Executive Director, Regulatory Affairs, Europe, slug=chris-ingram, email=, hs_updated_by_user_id=26433386}, third={}})
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      Barbara K.

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      Chris I.

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  • Read: Considerations for Your Pre-IND Meeting With the FDA Considerations for Your Pre-IND Meeting With the FDA

    Clinical Trials - Regulatory

    Considerations for Your Pre-IND Meeting With the FDA

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778884, hs_child_table_id=0, hs_updated_at=1709645745115, hs_published_at=1738849393727, description=Vann Parker is the Head of Regulatory Consultancy (North America) for Precision for Medicine. He received his PhD in Molecular Biology from The California Institute of Technology and spent the past 30 years supporting biopharmaceutical and drug development. He currently focuses on strategies for clinical development and interactions with FDA and other regulatory agencies. In addition to support of pre-IND activities, Vann has supported sponsors throughout the drug development process including applications for Fast Track, Breakthrough Therapy and Orphan Designations, formal meetings with FDA and full NDA/BLA submissions., avatar=Image{width=150,height=150,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/vann-parker.webp',altText='',fileId=null}, linkedin=https://www.linkedin.com/in/vann-parker-69565a6/, hs_name=, hs_path=, lastname=Parker, hs_initial_published_at=1716136551646, hs_created_at=1709645745115, hs_is_edited=false, hs_deleted_at=0, name=Vann, job=, slug=vann-parker, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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      Vann Parker

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  • Read: Inside a CRO: The Impact of a Biostatistician in Clinical Research Analyzing the Impact of a Biostatistician

    Clinical Trials

    Inside a CRO: The Impact of a Biostatistician in Clinical Research

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778868, hs_child_table_id=0, hs_updated_at=1715694281220, hs_published_at=1738849393727, description=Paul Pappas is a Senior Director of Biostatistics, bringing more than 20 years of experience to the team. His experience includes phase I-IV clinical trials as well as observational prospective cohort and registry studies. His therapeutic experience encompasses Autoimmune diseases, Cardiology, CNS, Infectious diseases, medical devices, Oncology, Rare diseases, and Vaccines. Paul has also co-authored over 30 manuscripts published in peer-reviewed medical journals., avatar=Image{width=626,height=710,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Paul-Pappas.png',altText='Paul-Pappas',fileId=167378452645}, linkedin=https://www.linkedin.com/in/paul-pappas-86176ab, hs_name=, hs_path=, lastname=Pappas, hs_initial_published_at=1716136551646, hs_created_at=1709645745099, hs_is_edited=false, hs_deleted_at=0, name=Paul, job=, slug=paul-pappas, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
    • Paul Pappas avatar

      Paul Pappas

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  • Read: Inside a CRO: The Critical Role of Regulatory and Startup Specialists in Clinical Research Inside a CRO: The Critical Role of Regulatory and Startup Specialists

    Clinical Trials - Regulatory - Early Phase Research

    Inside a CRO: The Critical Role of Regulatory and Startup Specialists in Clinical Research

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778850, hs_child_table_id=0, hs_updated_at=1709645745081, hs_published_at=1738849393727, description=Mar Galan is Sr. Start-up Line Manager for several EMEA countries at Precision. She has a Pharmacy Degree and a MSc in pharmaceutical industry and has spent over 16 years working in the CRO industry, mainly in the start-up area, in different roles. Mar’s experience covers for a wide variety of studies, from phase I to IV. Her well-rounded background spans multiple disease states across the various stages of drug development., avatar=Image{width=150,height=150,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/mar-galan.webp',altText='',fileId=null}, linkedin=https://www.linkedin.com/in/mar-galan-dalmau-9b068a1a, hs_name=, hs_path=, lastname=Galan, hs_initial_published_at=1716212769184, hs_created_at=1709645745081, hs_is_edited=false, hs_deleted_at=0, name=Mar, job=, slug=mar-galan, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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      Mar Galan

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  • Read: Case Study: International Phase 1 Non-small Cell Lung Cancer (NSCLC) Trial Case Study: International Phase 1 Non-small Cell Lung Cancer Trial

    Clinical Trials - Oncology

    Case Study: International Phase 1 Non-small Cell Lung Cancer (NSCLC) Trial

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=169567234066, hs_child_table_id=0, hs_updated_at=1723217613021, hs_published_at=1738849393727, description=Precision Experts are among the most experienced specialists in clinical research. We focus our hiring strategy on select indications to deliver excellence across each role. , avatar=Image{width=800,height=800,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Precision%20Expert.png',altText='Precision Expert',fileId=164175466823}, lastname=Experts, hs_initial_published_at=1718988967067, hs_created_by_user_id=26433386, hs_created_at=1717603871601, hs_is_edited=false, hs_deleted_at=0, name=Precision, slug=precision-experts, hs_updated_by_user_id=26433386}, second={}, third={}})
    • Precision Experts avatar

      Precision Experts

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  • Read: Clinical Trial Trends: Non-small Cell Lung Cancer (NSCLC) Clinical Trial Landscape: Non-small Cell Lung Cancer (NSCLC)

    Clinical Trials - Oncology

    Clinical Trial Trends: Non-small Cell Lung Cancer (NSCLC)

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778887, hs_child_table_id=0, hs_updated_at=1715690972359, hs_published_at=1738849393727, description=Andy Kinley, Ph.D. is Vice President of Innovation and Clinical Science at Precision for Medicine. He is a clinical researcher with over 25 years of combined experience leading basic and clinical research in oncology and hematology. His early scientific career focused on cancer cell signaling, setting a foundation to complement his clinical research roles in trial design and implementation of effective strategies for oncology clinical trials. Andy specializes in immuno-oncology trials (checkpoint inhibitors, T-cell agonists, bispecifics, cytokines, oncolytic viruses, neoantigen cancer vaccines), including autologous and allogeneic adoptive cell therapies (CAR-T, TCR, TIL, NK cells). Today, Andy identifies and implements innovative tools, datasets, and services that can impact clinical trial execution including quality, patient diversity, site identification, and trial timelines., avatar=Image{width=720,height=829,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/AndyKinley_headshot.png',altText='AndyKinley_headshot',fileId=167369936018}, linkedin=https://www.linkedin.com/in/andy-kinley-phd-5759551, hs_name=, hs_path=, lastname=Kinley, hs_initial_published_at=1716212769184, hs_created_at=1709645745118, hs_is_edited=false, hs_deleted_at=0, name=Andy, job=, slug=andy-kinley, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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      Andy Kinley

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  • Read: Inside a CRO: The Pivotal Role of Clinical Trial Manager in Clinical Research Inside a CRO - The Pivotal Role of Clinical Trial Manager in Clinical Research

    Clinical Trials

    Inside a CRO: The Pivotal Role of Clinical Trial Manager in Clinical Research

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778894, hs_child_table_id=0, hs_updated_at=1714461151531, hs_published_at=1738849393727, description=Vincent Shortino is a Principal Clinical Trial Manager, bringing more than 20 years of experience to Precision. His experience spans all major therapeutic areas with a heavy emphasis on Cardiovascular and Rare Indications, across Phases I–IV. He brings solid perspectives inclusive of sites, pharma and CROs from his previous roles of Study Coordinator, Site Director, CRA, and Clinical Trial Manager., avatar=Image{width=576,height=576,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Vincent%20Shortino.webp',altText='Vincent Shortino',fileId=165892429964}, linkedin=https://www.linkedin.com/in/vincent-shortino-954b3857, team=[{id=163080551773, name='Clinical Solutions Leadership'}], hs_name=, hs_path=, lastname=Shortino, hs_initial_published_at=1716212769184, hs_created_at=1709645745125, hs_is_edited=false, hs_deleted_at=0, name=Vincent, job=Principal Clinical Trial Manager, slug=vincent-shortino, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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      Vincent Shortino

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  • Read: Clinical Trial Patient Recruitment: Why Concierge Services are a Game-Changer Clinical Trial Patient Recruitment

    Clinical Trials - Early Phase Research - Rare Diseases

    Clinical Trial Patient Recruitment: Why Concierge Services are a Game-Changer

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778896, hs_child_table_id=0, hs_updated_at=1714461464701, hs_published_at=1738849393727, description=Sarabeth Velazquez is an Associate Director of Project Management at Precision for Medicine, having 20 years of experience in managing Phase I-III clinical trials. Sarabeth’s expertise covers a wide variety of therapeutic areas in rare disease, oncology, dermatology, ophthalmology and cosmetic clinical trials. Her experience notably includes: abdominal bulging, submental subcutaneous fat, molluscum contagiosum, onychomycosis, neurofibromas, herpes labialis, hyperhidrosis, breast implants, colorectal cancer, solid tumors, breast cancer, ovarian cancer, lymphoma, cataracts, pulmonary arterial hypertension, classic galactosemia, and sorbitol dehydrogenase deficiency., avatar=Image{width=576,height=576,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Sarabeth%20Velasquez%20Square.webp',altText='Sarabeth Velasquez Square',fileId=165892429960}, linkedin=https://www.linkedin.com/in/sarabeth-alcala-velazquez-17409811/, hs_name=, hs_path=, lastname=Velazquez, hs_initial_published_at=1716212769184, hs_created_at=1709645745127, hs_is_edited=false, hs_deleted_at=0, name=Sarabeth, job=, slug=sarabeth-velazquez, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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      Sarabeth Velazquez

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  • Read: CROs in Clinical Trials: Keys to Successful Sponsor-CRO Partnerships CROs in Clinical Trials

    Clinical Trials - Early Phase Research

    CROs in Clinical Trials: Keys to Successful Sponsor-CRO Partnerships

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778858, hs_child_table_id=0, hs_updated_at=1736540179119, hs_published_at=1738849393727, description=Rob Maiale is an innovative marketing leader and creative technologist who transforms complex healthcare challenges into meaningful, impactful stories. With over 15 years of experience across clinical and translational research, patient education, pharmaceuticals, and diagnostics, he merges cutting-edge technology with inspired storytelling to build award-winning brand narratives. At Precision, Rob collaborates with leading experts to translate deep scientific expertise into accessible, engaging, and culturally resonant content—connecting audiences to the future of life-changing research., avatar=Image{width=400,height=400,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Rob%20Maiale.jpg',altText='Rob Maiale',fileId=184765575245}, linkedin=https://www.linkedin.com/in/rob-maiale/, hs_name=, hs_path=, lastname=Maiale, hs_initial_published_at=1729783715853, hs_created_at=1709645745089, hs_is_edited=false, hs_deleted_at=0, name=Rob, job=, slug=rob-maiale, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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      Rob Maiale

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  • Read: Phase I Clinical Trial Designs: Backfill i3+3 (Bi3+3) Clinical Trial Designs

    Clinical Trials - Early Phase Research - Oncology

    Phase I Clinical Trial Designs: Backfill i3+3 (Bi3+3)

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778891, hs_child_table_id=0, hs_updated_at=1709645745122, hs_published_at=1738849393727, description=Kurt Preugschat has over 11 years of statistical experience from Phase I to Phase IV clinical trials. He is a lead statistician, providing statistical support and oversight for numerous clinical trials associated with new drug applications (NDA), supplemental new drug applications (sNDA), and medical devices. His expertise includes the development of study designs to meet complex clinical questions and the measurement of desired outcomes. In addition, Kurt has extensive experience generating statistical analyses and creating complex SAS programs and macros used by study team., avatar=Image{width=150,height=150,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/kurt-preugschat.webp',altText='',fileId=null}, linkedin=https://www.linkedin.com/in/kurt-preugschat-97298923a, hs_name=, hs_path=, lastname=Preugschat, hs_initial_published_at=1716136551646, hs_created_at=1709645745122, hs_is_edited=false, hs_deleted_at=0, name=Kurt, job=, slug=kurt-preugschat, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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      Kurt Preugschat

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  • Read: Inside a CRO: The Critical Role of Clinical Data Managers in Clinical Research Clinical Data Managers

    Clinical Trials - Data Intelligence

    Inside a CRO: The Critical Role of Clinical Data Managers in Clinical Research

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=169567234066, hs_child_table_id=0, hs_updated_at=1723217613021, hs_published_at=1738849393727, description=Precision Experts are among the most experienced specialists in clinical research. We focus our hiring strategy on select indications to deliver excellence across each role. , avatar=Image{width=800,height=800,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Precision%20Expert.png',altText='Precision Expert',fileId=164175466823}, lastname=Experts, hs_initial_published_at=1718988967067, hs_created_by_user_id=26433386, hs_created_at=1717603871601, hs_is_edited=false, hs_deleted_at=0, name=Precision, slug=precision-experts, hs_updated_by_user_id=26433386}, second={}, third={}})
    • Precision Experts avatar

      Precision Experts

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  • Read: Inside a CRO: The Essential Role of a Clinical Project Manager inside a cro

    Clinical Trials

    Inside a CRO: The Essential Role of a Clinical Project Manager

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778873, hs_child_table_id=0, hs_updated_at=1715693354219, hs_published_at=1738849393727, description=Lindsey Pierce, PhD is a Senior Project Manager with over 15 years of research experience, ranging from diagnostic development and patent acquisition, to genomic medicine advancements in viral and pathogen genotyping, and clinical research. She has successfully managed both local and global projects across many programs and therapeutic areas. While specializing in early phase oncology, she also has worked in late phase oncology trials as well as rare disease studies. Her passion is to bring treatment to patients in need to help them battle the unfortunate and let the family know that research is on their side every step of the way., avatar=Image{width=710,height=710,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Lindsey-Pierce.png',altText='Lindsey-Pierce',fileId=167373615946}, linkedin=https://www.linkedin.com/in/lindsey-pierce-phd-a252b812b, hs_name=, hs_path=, lastname=Pierce, hs_initial_published_at=1716212769184, hs_created_at=1709645745104, hs_is_edited=false, hs_deleted_at=0, name=Lindsey, job=, slug=lindsey-pierce, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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      Lindsey Pierce

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  • Read: Phase III Case Study: Adapting in the Face of Adversity Phase III Case Study

    Clinical Trials

    Phase III Case Study: Adapting in the Face of Adversity

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778845, hs_child_table_id=0, hs_updated_at=1709645745076, hs_published_at=1738849393727, description=Brian Beus is a Principal Biostatistician with more than 25 years experience supporting the statistical analysis of data through all phases of clinical trials across many therapeutic areas. He has extensive experience in leading teams and working with sponsors through study design, protocol development, adaptive design, statistical analysis plans, statistical analysis, clinical study reports, regulatory submissions, and regulatory responses., avatar=Image{width=150,height=150,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/brian-beus.webp',altText='',fileId=null}, linkedin=https://www.linkedin.com/in/brian-beus-66033333, hs_name=, hs_path=, lastname=Beus, hs_initial_published_at=1716212769184, hs_created_at=1709645745076, hs_is_edited=false, hs_deleted_at=0, name=Brian, job=, slug=brian-beus, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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      Brian Beus

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  • Read: Controlled Substances in EU Clinical Trials Controlled Substances in EU Clinical Trials

    Clinical Trials - Regulatory

    Controlled Substances in EU Clinical Trials

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778862, hs_child_table_id=0, hs_updated_at=1709645745093, hs_published_at=1738849393727, description=Olya Demireva is a Senior CTM bringing over 15 years of experience. She is a certified psychiatrist and clinical immunologist with 15 years of clinical research in CNS diseases and solid medical scientific background in biological psychiatry with focus on Major Depression and Bipolar Disorders, and neuro-psycho-immunology. Her experience in clinical research spans over almost all therapeutic areas with emphasis on Oncology, Pulmonology, Cardiovascular Diseases, Sleep Disorders, Hematology, Endocrinology and Rare Diseases across phases I-IV., avatar=Image{width=150,height=150,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/olya-demireva.webp',altText='',fileId=null}, linkedin=https://www.linkedin.com/in/olya-demireva-md-0a91809, hs_name=, hs_path=, lastname=Demireva, hs_initial_published_at=1716136551646, hs_created_at=1709645745093, hs_is_edited=false, hs_deleted_at=0, name=Olya, job=, slug=olya-demireva, email=, hs_updated_by_user_id=26433386}, second={hs_id=159488778847, hs_child_table_id=0, hs_updated_at=1714461476003, hs_published_at=1738849393727, description=Saoussen Brun is a Senior Director of Project Management at Precision for Medicine. She brings more than 18 years of Clinical and Project Management experience to the Precision team. Saoussen’s expertise covers a wide variety of therapeutic areas, with strong experience in oncology and neurology indication. She leads and motivates high-performing teams under tough deadlines to meet both project goals and company targets., avatar=Image{width=576,height=576,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Saoussen%20Brun%20Square.webp',altText='Saoussen Brun Square',fileId=165892742326}, linkedin=https://www.linkedin.com/in/saoussen-bouali-brun-phd-2212b852, hs_name=, hs_path=, lastname=Brun, hs_initial_published_at=1716212769184, hs_created_at=1709645745078, hs_is_edited=false, hs_deleted_at=0, name=Saoussen, job=, slug=saoussen-brun, email=, hs_updated_by_user_id=26433386}, third={}})
    • Olya D. avatar

      Olya D.

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  • Read: Incorporating Decentralized Clinical Trial Strategies into CNS Studies Incorporating Decentralized Clinical Trial

    Clinical Trials

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778843, hs_child_table_id=0, hs_updated_at=1714461297945, hs_published_at=1738849393727, description=Robert Bauer is an Executive Director of Operational Strategy at Precision with over 20 years of clinical trial operations experience from both the sponsor and CRO perspectives. He has led teams in the conduct of trials from Phase I through IV and has experience across a wide variety of trial designs. Bob has experience across many therapeutic areas some of which include rare diseases, oncology, depression, schizophrenia, and substance use disorders., avatar=Image{width=576,height=576,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Robert%20Bauer%20Square.webp',altText='Robert Bauer Square',fileId=165892429961}, linkedin=https://www.linkedin.com/in/robert-bauer-a78b704b, hs_name=, hs_path=, lastname=Bauer, hs_initial_published_at=1716212769184, hs_created_at=1709645745074, hs_is_edited=false, hs_deleted_at=0, name=Robert, job=, slug=robert-bauer, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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    Clinical Trials - Regulatory - Rare Diseases

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778884, hs_child_table_id=0, hs_updated_at=1709645745115, hs_published_at=1738849393727, description=Vann Parker is the Head of Regulatory Consultancy (North America) for Precision for Medicine. He received his PhD in Molecular Biology from The California Institute of Technology and spent the past 30 years supporting biopharmaceutical and drug development. He currently focuses on strategies for clinical development and interactions with FDA and other regulatory agencies. In addition to support of pre-IND activities, Vann has supported sponsors throughout the drug development process including applications for Fast Track, Breakthrough Therapy and Orphan Designations, formal meetings with FDA and full NDA/BLA submissions., avatar=Image{width=150,height=150,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/vann-parker.webp',altText='',fileId=null}, linkedin=https://www.linkedin.com/in/vann-parker-69565a6/, hs_name=, hs_path=, lastname=Parker, hs_initial_published_at=1716136551646, hs_created_at=1709645745115, hs_is_edited=false, hs_deleted_at=0, name=Vann, job=, slug=vann-parker, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: Overcoming Hurdles in Rare Disease Research and Development Rare Disease Research and Development

    Clinical Trials - Regulatory - Rare Diseases

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778858, hs_child_table_id=0, hs_updated_at=1736540179119, hs_published_at=1738849393727, description=Rob Maiale is an innovative marketing leader and creative technologist who transforms complex healthcare challenges into meaningful, impactful stories. With over 15 years of experience across clinical and translational research, patient education, pharmaceuticals, and diagnostics, he merges cutting-edge technology with inspired storytelling to build award-winning brand narratives. At Precision, Rob collaborates with leading experts to translate deep scientific expertise into accessible, engaging, and culturally resonant content—connecting audiences to the future of life-changing research., avatar=Image{width=400,height=400,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Rob%20Maiale.jpg',altText='Rob Maiale',fileId=184765575245}, linkedin=https://www.linkedin.com/in/rob-maiale/, hs_name=, hs_path=, lastname=Maiale, hs_initial_published_at=1729783715853, hs_created_at=1709645745089, hs_is_edited=false, hs_deleted_at=0, name=Rob, job=, slug=rob-maiale, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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      Rob Maiale

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    Clinical Trials - Regulatory - Oncology

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778884, hs_child_table_id=0, hs_updated_at=1709645745115, hs_published_at=1738849393727, description=Vann Parker is the Head of Regulatory Consultancy (North America) for Precision for Medicine. He received his PhD in Molecular Biology from The California Institute of Technology and spent the past 30 years supporting biopharmaceutical and drug development. He currently focuses on strategies for clinical development and interactions with FDA and other regulatory agencies. In addition to support of pre-IND activities, Vann has supported sponsors throughout the drug development process including applications for Fast Track, Breakthrough Therapy and Orphan Designations, formal meetings with FDA and full NDA/BLA submissions., avatar=Image{width=150,height=150,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/vann-parker.webp',altText='',fileId=null}, linkedin=https://www.linkedin.com/in/vann-parker-69565a6/, hs_name=, hs_path=, lastname=Parker, hs_initial_published_at=1716136551646, hs_created_at=1709645745115, hs_is_edited=false, hs_deleted_at=0, name=Vann, job=, slug=vann-parker, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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    Clinical Trials - Rare Diseases

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778894, hs_child_table_id=0, hs_updated_at=1714461151531, hs_published_at=1738849393727, description=Vincent Shortino is a Principal Clinical Trial Manager, bringing more than 20 years of experience to Precision. His experience spans all major therapeutic areas with a heavy emphasis on Cardiovascular and Rare Indications, across Phases I–IV. He brings solid perspectives inclusive of sites, pharma and CROs from his previous roles of Study Coordinator, Site Director, CRA, and Clinical Trial Manager., avatar=Image{width=576,height=576,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Vincent%20Shortino.webp',altText='Vincent Shortino',fileId=165892429964}, linkedin=https://www.linkedin.com/in/vincent-shortino-954b3857, team=[{id=163080551773, name='Clinical Solutions Leadership'}], hs_name=, hs_path=, lastname=Shortino, hs_initial_published_at=1716212769184, hs_created_at=1709645745125, hs_is_edited=false, hs_deleted_at=0, name=Vincent, job=Principal Clinical Trial Manager, slug=vincent-shortino, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: Centralized vs Decentralized Raters: When to Use Which in CNS Trials? Centralized vs Decentralized Raters

    Clinical Trials

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778858, hs_child_table_id=0, hs_updated_at=1736540179119, hs_published_at=1738849393727, description=Rob Maiale is an innovative marketing leader and creative technologist who transforms complex healthcare challenges into meaningful, impactful stories. With over 15 years of experience across clinical and translational research, patient education, pharmaceuticals, and diagnostics, he merges cutting-edge technology with inspired storytelling to build award-winning brand narratives. At Precision, Rob collaborates with leading experts to translate deep scientific expertise into accessible, engaging, and culturally resonant content—connecting audiences to the future of life-changing research., avatar=Image{width=400,height=400,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Rob%20Maiale.jpg',altText='Rob Maiale',fileId=184765575245}, linkedin=https://www.linkedin.com/in/rob-maiale/, hs_name=, hs_path=, lastname=Maiale, hs_initial_published_at=1729783715853, hs_created_at=1709645745089, hs_is_edited=false, hs_deleted_at=0, name=Rob, job=, slug=rob-maiale, email=, hs_updated_by_user_id=26433386}, second={hs_id=159488778894, hs_child_table_id=0, hs_updated_at=1714461151531, hs_published_at=1738849393727, description=Vincent Shortino is a Principal Clinical Trial Manager, bringing more than 20 years of experience to Precision. His experience spans all major therapeutic areas with a heavy emphasis on Cardiovascular and Rare Indications, across Phases I–IV. He brings solid perspectives inclusive of sites, pharma and CROs from his previous roles of Study Coordinator, Site Director, CRA, and Clinical Trial Manager., avatar=Image{width=576,height=576,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Vincent%20Shortino.webp',altText='Vincent Shortino',fileId=165892429964}, linkedin=https://www.linkedin.com/in/vincent-shortino-954b3857, team=[{id=163080551773, name='Clinical Solutions Leadership'}], hs_name=, hs_path=, lastname=Shortino, hs_initial_published_at=1716212769184, hs_created_at=1709645745125, hs_is_edited=false, hs_deleted_at=0, name=Vincent, job=Principal Clinical Trial Manager, slug=vincent-shortino, email=, hs_updated_by_user_id=26433386}, third={}})
    • Rob M. avatar

      Rob M.

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      Vincent S.

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  • Read: Pros and Cons: Innovative Study Designs vs. Traditional FIH Study Designs vs. Traditional FIH

    Clinical Trials

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778854, hs_child_table_id=0, hs_updated_at=1715695005945, hs_published_at=1738849393727, description=Rosa Canals López has 15 years of experience in managing Phase I-IV clinical trials, including >7 years of Clinical Management experience. Her focus is on Phase I studies and CAR-T, with additional experience in oncology, hematology, pediatrics, infectious diseases, cardiology, and nephrology., avatar=Image{width=533,height=710,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Rosa-Canals.png',altText='Rosa-Canals',fileId=167374630834}, linkedin=https://www.linkedin.com/in/rosa-maria-canals-l%C3%B3pez-74902194, hs_name=, hs_path=, lastname=Canals López, hs_initial_published_at=1716136551646, hs_created_at=1709645745085, hs_is_edited=false, hs_deleted_at=0, name=Rosa, job=, slug=rosa-canals-lópez, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: Overview: Innovative Study Designs vs. Traditional FIH Innovative Study Designs vs. Traditional FIH

    Clinical Trials

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778854, hs_child_table_id=0, hs_updated_at=1715695005945, hs_published_at=1738849393727, description=Rosa Canals López has 15 years of experience in managing Phase I-IV clinical trials, including >7 years of Clinical Management experience. Her focus is on Phase I studies and CAR-T, with additional experience in oncology, hematology, pediatrics, infectious diseases, cardiology, and nephrology., avatar=Image{width=533,height=710,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Rosa-Canals.png',altText='Rosa-Canals',fileId=167374630834}, linkedin=https://www.linkedin.com/in/rosa-maria-canals-l%C3%B3pez-74902194, hs_name=, hs_path=, lastname=Canals López, hs_initial_published_at=1716136551646, hs_created_at=1709645745085, hs_is_edited=false, hs_deleted_at=0, name=Rosa, job=, slug=rosa-canals-lópez, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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      Rosa Canals López

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  • Read: Advancing the Use of Biomarkers in CNS Drug Discovery and Development Biomarkers in CNS Drug Discovery and Development

    Clinical Trials - Biomarkers

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778867, hs_child_table_id=0, hs_updated_at=1714461162887, hs_published_at=1738849393727, description=Tracey Owens is a Director of Project and Clinical Trial Management at Precision, having 28 years of experience in managing Phase I-IV clinical trials. Tracey is highly experienced in providing directional oversight on rare disease, CNS, psychiatric and oncology clinical trials. Her experience notably includes: ALS, bipolar disorder, epilepsy, major depressive disorder, schizophrenia, idiopathic hypersomnia, CIDP, traumatic brain injury, multiple myeloma and dementia (including Alzheimer’s and Parkinson’s Disease.), avatar=Image{width=576,height=576,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Tracey%20Owens.webp',altText='Tracey Owens',fileId=165892372604}, linkedin=https://www.linkedin.com/in/trowens, hs_name=, hs_path=, lastname=Owens, hs_initial_published_at=1716212769184, hs_created_at=1709645745098, hs_is_edited=false, hs_deleted_at=0, name=Tracey, job=, slug=tracey-owens, email=, hs_updated_by_user_id=26433386}, second={hs_id=159488778894, hs_child_table_id=0, hs_updated_at=1714461151531, hs_published_at=1738849393727, description=Vincent Shortino is a Principal Clinical Trial Manager, bringing more than 20 years of experience to Precision. His experience spans all major therapeutic areas with a heavy emphasis on Cardiovascular and Rare Indications, across Phases I–IV. He brings solid perspectives inclusive of sites, pharma and CROs from his previous roles of Study Coordinator, Site Director, CRA, and Clinical Trial Manager., avatar=Image{width=576,height=576,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Vincent%20Shortino.webp',altText='Vincent Shortino',fileId=165892429964}, linkedin=https://www.linkedin.com/in/vincent-shortino-954b3857, team=[{id=163080551773, name='Clinical Solutions Leadership'}], hs_name=, hs_path=, lastname=Shortino, hs_initial_published_at=1716212769184, hs_created_at=1709645745125, hs_is_edited=false, hs_deleted_at=0, name=Vincent, job=Principal Clinical Trial Manager, slug=vincent-shortino, email=, hs_updated_by_user_id=26433386}, third={}})
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      Tracey O.

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      Vincent S.

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  • Read: Five Considerations for Global Phase 3 Trials in Oncology Global Phase 3 Trials in Oncology

    Clinical Trials - Regulatory - Oncology

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=169567234066, hs_child_table_id=0, hs_updated_at=1723217613021, hs_published_at=1738849393727, description=Precision Experts are among the most experienced specialists in clinical research. We focus our hiring strategy on select indications to deliver excellence across each role. , avatar=Image{width=800,height=800,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Precision%20Expert.png',altText='Precision Expert',fileId=164175466823}, lastname=Experts, hs_initial_published_at=1718988967067, hs_created_by_user_id=26433386, hs_created_at=1717603871601, hs_is_edited=false, hs_deleted_at=0, name=Precision, slug=precision-experts, hs_updated_by_user_id=26433386}, second={}, third={}})
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      Precision Experts

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  • Read: Using electronic patient-reported outcome (ePRO) technology to address key challenges in CNS trials ePRO technology

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778867, hs_child_table_id=0, hs_updated_at=1714461162887, hs_published_at=1738849393727, description=Tracey Owens is a Director of Project and Clinical Trial Management at Precision, having 28 years of experience in managing Phase I-IV clinical trials. Tracey is highly experienced in providing directional oversight on rare disease, CNS, psychiatric and oncology clinical trials. Her experience notably includes: ALS, bipolar disorder, epilepsy, major depressive disorder, schizophrenia, idiopathic hypersomnia, CIDP, traumatic brain injury, multiple myeloma and dementia (including Alzheimer’s and Parkinson’s Disease.), avatar=Image{width=576,height=576,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Tracey%20Owens.webp',altText='Tracey Owens',fileId=165892372604}, linkedin=https://www.linkedin.com/in/trowens, hs_name=, hs_path=, lastname=Owens, hs_initial_published_at=1716212769184, hs_created_at=1709645745098, hs_is_edited=false, hs_deleted_at=0, name=Tracey, job=, slug=tracey-owens, email=, hs_updated_by_user_id=26433386}, second={hs_id=159488778894, hs_child_table_id=0, hs_updated_at=1714461151531, hs_published_at=1738849393727, description=Vincent Shortino is a Principal Clinical Trial Manager, bringing more than 20 years of experience to Precision. His experience spans all major therapeutic areas with a heavy emphasis on Cardiovascular and Rare Indications, across Phases I–IV. He brings solid perspectives inclusive of sites, pharma and CROs from his previous roles of Study Coordinator, Site Director, CRA, and Clinical Trial Manager., avatar=Image{width=576,height=576,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Vincent%20Shortino.webp',altText='Vincent Shortino',fileId=165892429964}, linkedin=https://www.linkedin.com/in/vincent-shortino-954b3857, team=[{id=163080551773, name='Clinical Solutions Leadership'}], hs_name=, hs_path=, lastname=Shortino, hs_initial_published_at=1716212769184, hs_created_at=1709645745125, hs_is_edited=false, hs_deleted_at=0, name=Vincent, job=Principal Clinical Trial Manager, slug=vincent-shortino, email=, hs_updated_by_user_id=26433386}, third={}})
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      Tracey O.

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      Vincent S.

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  • Read: R&D Tax Incentive Program Support R&D Tax Incentive Program Support

    Clinical Trials

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778892, hs_child_table_id=0, hs_updated_at=1715691877459, hs_published_at=1738849393727, description=Estelle Roger is a senior program manager at Precision Medicine Group and supports strategies related to public funding of research and innovation. With more than 5 years building and managing R&D Tax incentives strategies for both CROs and pharmaceutical industries, Estelle’s expertise covers a meaningful panel of R&D tax relief regimes across North America and Europe., avatar=Image{width=720,height=812,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Estelle-roger.png',altText='Estelle-roger',fileId=167371301904}, linkedin=https://www.linkedin.com/in/estelle-roger-n, hs_name=, hs_path=, lastname=Roger, hs_initial_published_at=1716212769184, hs_created_at=1709645745123, hs_is_edited=false, hs_deleted_at=0, name=Estelle, job=, slug=estelle-roger, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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      Estelle Roger

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  • Read: Increased Complexity and Therapeutic Combinations Pave the Way in Immuno-oncology Increased Complexity and Therapeutic Combinations Pave the Way in Immuno-oncology

    Clinical Trials - Oncology

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778887, hs_child_table_id=0, hs_updated_at=1715690972359, hs_published_at=1738849393727, description=Andy Kinley, Ph.D. is Vice President of Innovation and Clinical Science at Precision for Medicine. He is a clinical researcher with over 25 years of combined experience leading basic and clinical research in oncology and hematology. His early scientific career focused on cancer cell signaling, setting a foundation to complement his clinical research roles in trial design and implementation of effective strategies for oncology clinical trials. Andy specializes in immuno-oncology trials (checkpoint inhibitors, T-cell agonists, bispecifics, cytokines, oncolytic viruses, neoantigen cancer vaccines), including autologous and allogeneic adoptive cell therapies (CAR-T, TCR, TIL, NK cells). Today, Andy identifies and implements innovative tools, datasets, and services that can impact clinical trial execution including quality, patient diversity, site identification, and trial timelines., avatar=Image{width=720,height=829,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/AndyKinley_headshot.png',altText='AndyKinley_headshot',fileId=167369936018}, linkedin=https://www.linkedin.com/in/andy-kinley-phd-5759551, hs_name=, hs_path=, lastname=Kinley, hs_initial_published_at=1716212769184, hs_created_at=1709645745118, hs_is_edited=false, hs_deleted_at=0, name=Andy, job=, slug=andy-kinley, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: FDA Procedural Guidance: Expansion Cohorts in FIH Oncology Clinical Trials FDA Procedural Guidance: Expansion Cohorts in FIH Oncology Clinical Trials

    Clinical Trials - Rare Diseases

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778884, hs_child_table_id=0, hs_updated_at=1709645745115, hs_published_at=1738849393727, description=Vann Parker is the Head of Regulatory Consultancy (North America) for Precision for Medicine. He received his PhD in Molecular Biology from The California Institute of Technology and spent the past 30 years supporting biopharmaceutical and drug development. He currently focuses on strategies for clinical development and interactions with FDA and other regulatory agencies. In addition to support of pre-IND activities, Vann has supported sponsors throughout the drug development process including applications for Fast Track, Breakthrough Therapy and Orphan Designations, formal meetings with FDA and full NDA/BLA submissions., avatar=Image{width=150,height=150,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/vann-parker.webp',altText='',fileId=null}, linkedin=https://www.linkedin.com/in/vann-parker-69565a6/, hs_name=, hs_path=, lastname=Parker, hs_initial_published_at=1716136551646, hs_created_at=1709645745115, hs_is_edited=false, hs_deleted_at=0, name=Vann, job=, slug=vann-parker, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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      Vann Parker

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  • Read: Key Considerations for Selecting a CRO Partner CRO

    Clinical Trials

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778866, hs_child_table_id=0, hs_updated_at=1716212949488, hs_published_at=1738849393727, description=Frances Murphy is a leading authority in clinical CROs, focused on client services and regional growth implementation. Murphy is a dedicated proponent of harnessing truly personalized medicine to develop more effective treatments for patients and brings a high ethical standard to discussions and values transparency and collaboration., avatar=Image{width=576,height=576,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Frances%20Murphy.webp',altText='Frances Murphy',fileId=164429952326}, linkedin=https://www.linkedin.com/in/frances-murphy-24800112, hs_name=, hs_path=, lastname=Murphy, hs_initial_published_at=1716213113382, hs_created_at=1709645745097, hs_is_edited=false, hs_deleted_at=0, name=Frances, job=Regional Vice President, Clinical Business Solutions, EU & APAC, slug=frances-murphy, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: Why Caregivers Are the Key to Patient-Centric Clinical Trials Why Caregivers Are the Key to Patient-Centric Clinical Trials

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778858, hs_child_table_id=0, hs_updated_at=1736540179119, hs_published_at=1738849393727, description=Rob Maiale is an innovative marketing leader and creative technologist who transforms complex healthcare challenges into meaningful, impactful stories. With over 15 years of experience across clinical and translational research, patient education, pharmaceuticals, and diagnostics, he merges cutting-edge technology with inspired storytelling to build award-winning brand narratives. At Precision, Rob collaborates with leading experts to translate deep scientific expertise into accessible, engaging, and culturally resonant content—connecting audiences to the future of life-changing research., avatar=Image{width=400,height=400,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Rob%20Maiale.jpg',altText='Rob Maiale',fileId=184765575245}, linkedin=https://www.linkedin.com/in/rob-maiale/, hs_name=, hs_path=, lastname=Maiale, hs_initial_published_at=1729783715853, hs_created_at=1709645745089, hs_is_edited=false, hs_deleted_at=0, name=Rob, job=, slug=rob-maiale, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: Leveraging genetic laboratories in rare disease patient identification genetic laboratories

    Clinical Trials - Early Phase Research - Rare Diseases

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778858, hs_child_table_id=0, hs_updated_at=1736540179119, hs_published_at=1738849393727, description=Rob Maiale is an innovative marketing leader and creative technologist who transforms complex healthcare challenges into meaningful, impactful stories. With over 15 years of experience across clinical and translational research, patient education, pharmaceuticals, and diagnostics, he merges cutting-edge technology with inspired storytelling to build award-winning brand narratives. At Precision, Rob collaborates with leading experts to translate deep scientific expertise into accessible, engaging, and culturally resonant content—connecting audiences to the future of life-changing research., avatar=Image{width=400,height=400,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Rob%20Maiale.jpg',altText='Rob Maiale',fileId=184765575245}, linkedin=https://www.linkedin.com/in/rob-maiale/, hs_name=, hs_path=, lastname=Maiale, hs_initial_published_at=1729783715853, hs_created_at=1709645745089, hs_is_edited=false, hs_deleted_at=0, name=Rob, job=, slug=rob-maiale, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=169567234066, hs_child_table_id=0, hs_updated_at=1723217613021, hs_published_at=1738849393727, description=Precision Experts are among the most experienced specialists in clinical research. We focus our hiring strategy on select indications to deliver excellence across each role. , avatar=Image{width=800,height=800,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Precision%20Expert.png',altText='Precision Expert',fileId=164175466823}, lastname=Experts, hs_initial_published_at=1718988967067, hs_created_by_user_id=26433386, hs_created_at=1717603871601, hs_is_edited=false, hs_deleted_at=0, name=Precision, slug=precision-experts, hs_updated_by_user_id=26433386}, second={}, third={}})
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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=169567234066, hs_child_table_id=0, hs_updated_at=1723217613021, hs_published_at=1738849393727, description=Precision Experts are among the most experienced specialists in clinical research. We focus our hiring strategy on select indications to deliver excellence across each role. , avatar=Image{width=800,height=800,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Precision%20Expert.png',altText='Precision Expert',fileId=164175466823}, lastname=Experts, hs_initial_published_at=1718988967067, hs_created_by_user_id=26433386, hs_created_at=1717603871601, hs_is_edited=false, hs_deleted_at=0, name=Precision, slug=precision-experts, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: Improving Data Quality with Clinical Science Analytics & Insights Improving Data Quality with Clinical Science Analytics & Insights

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778864, hs_child_table_id=0, hs_updated_at=1714461642203, hs_published_at=1738849393727, description=Chris Monaco has thirty-five years of expertise in the clinical research and pharmaceutical services industry supporting Phase I-IV clinical trials across a variety of therapeutic areas, including FIH, P1/2, dose escalation, and expansion oncology clinical trials. Currently, she is responsible for the administrative management of CSAI-Oncology Solutions services at both the department and team levels, driving process improvements for consistent quality across deliverables. Additionally, Chris supports business operations, resource management, and JReview implementation for applicable clients. Her passion shines through her leadership, commitment to excellence, and service delivery., avatar=Image{width=576,height=576,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Chris%20Monaco.webp',altText='Chris Monaco',fileId=165892809105}, linkedin=https://www.linkedin.com/in/christine-monaco-812a879, hs_name=, hs_path=, lastname=Monaco, hs_initial_published_at=1716212769184, hs_created_at=1709645745095, hs_is_edited=false, hs_deleted_at=0, name=Chris, job=, slug=chris-monaco, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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    Clinical Trials - Early Phase Research

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778887, hs_child_table_id=0, hs_updated_at=1715690972359, hs_published_at=1738849393727, description=Andy Kinley, Ph.D. is Vice President of Innovation and Clinical Science at Precision for Medicine. He is a clinical researcher with over 25 years of combined experience leading basic and clinical research in oncology and hematology. His early scientific career focused on cancer cell signaling, setting a foundation to complement his clinical research roles in trial design and implementation of effective strategies for oncology clinical trials. Andy specializes in immuno-oncology trials (checkpoint inhibitors, T-cell agonists, bispecifics, cytokines, oncolytic viruses, neoantigen cancer vaccines), including autologous and allogeneic adoptive cell therapies (CAR-T, TCR, TIL, NK cells). Today, Andy identifies and implements innovative tools, datasets, and services that can impact clinical trial execution including quality, patient diversity, site identification, and trial timelines., avatar=Image{width=720,height=829,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/AndyKinley_headshot.png',altText='AndyKinley_headshot',fileId=167369936018}, linkedin=https://www.linkedin.com/in/andy-kinley-phd-5759551, hs_name=, hs_path=, lastname=Kinley, hs_initial_published_at=1716212769184, hs_created_at=1709645745118, hs_is_edited=false, hs_deleted_at=0, name=Andy, job=, slug=andy-kinley, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: Inside a CRO: Logistics Coordinators Are Vital to Cell and Gene Trial Success Why Logistics Coordinators Are Vital to Cell and Gene Trial Success

    Manufacturing - Cell Therapies - Gene Therapies

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778857, hs_child_table_id=0, hs_updated_at=1709645745088, hs_published_at=1738849393727, description=Tiziana Magnani is a Senior Project Manager at Precision in Milan, Italy. She has dedicated more than 20 years to project management and clinical research in different settings and brings more than 15 years of experience in the academic world and in the management of large multi-professional teams to Precision., avatar=Image{width=150,height=150,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/tiziana-magnani.webp',altText='',fileId=null}, linkedin=https://www.linkedin.com/in/tiziana-magnani-a9b288a, hs_name=, hs_path=, lastname=Magnani, hs_initial_published_at=1716212769184, hs_created_at=1709645745088, hs_is_edited=false, hs_deleted_at=0, name=Tiziana, job=, slug=tiziana-magnani, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: Long-term Follow-up Studies: Gene Therapy Products, Protocols and Potential Issues Long-term Follow-up Studies: Gene Therapy Products, Protocols and Potential Issues

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778871, hs_child_table_id=0, hs_updated_at=1709645745102, hs_published_at=1738849393727, description=Meredith Latino is the Director of Medical Writing at Precision for Medicine. She earned a PhD in Molecular and Cellular Biology from Tulane University and brings more than 16 years of experience to the Precision team, including 9 years of medical writing and 8 years of academic research/writing., avatar=Image{width=150,height=150,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/meredith-latino.webp',altText='',fileId=null}, linkedin=https://www.linkedin.com/in/meredith-latino-7a2bba119/, hs_name=, hs_path=, lastname=Latino, hs_initial_published_at=1716212769184, hs_created_at=1709645745102, hs_is_edited=false, hs_deleted_at=0, name=Meredith, job=, slug=meredith-latino, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: Clinical Data Management: Data Integration vs. Data Reconciliation clinical data management

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=169567234066, hs_child_table_id=0, hs_updated_at=1723217613021, hs_published_at=1738849393727, description=Precision Experts are among the most experienced specialists in clinical research. We focus our hiring strategy on select indications to deliver excellence across each role. , avatar=Image{width=800,height=800,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Precision%20Expert.png',altText='Precision Expert',fileId=164175466823}, lastname=Experts, hs_initial_published_at=1718988967067, hs_created_by_user_id=26433386, hs_created_at=1717603871601, hs_is_edited=false, hs_deleted_at=0, name=Precision, slug=precision-experts, hs_updated_by_user_id=26433386}, second={}, third={}})
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    Clinical Trials - Early Phase Research - Rare Diseases

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778858, hs_child_table_id=0, hs_updated_at=1736540179119, hs_published_at=1738849393727, description=Rob Maiale is an innovative marketing leader and creative technologist who transforms complex healthcare challenges into meaningful, impactful stories. With over 15 years of experience across clinical and translational research, patient education, pharmaceuticals, and diagnostics, he merges cutting-edge technology with inspired storytelling to build award-winning brand narratives. At Precision, Rob collaborates with leading experts to translate deep scientific expertise into accessible, engaging, and culturally resonant content—connecting audiences to the future of life-changing research., avatar=Image{width=400,height=400,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Rob%20Maiale.jpg',altText='Rob Maiale',fileId=184765575245}, linkedin=https://www.linkedin.com/in/rob-maiale/, hs_name=, hs_path=, lastname=Maiale, hs_initial_published_at=1729783715853, hs_created_at=1709645745089, hs_is_edited=false, hs_deleted_at=0, name=Rob, job=, slug=rob-maiale, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778857, hs_child_table_id=0, hs_updated_at=1709645745088, hs_published_at=1738849393727, description=Tiziana Magnani is a Senior Project Manager at Precision in Milan, Italy. She has dedicated more than 20 years to project management and clinical research in different settings and brings more than 15 years of experience in the academic world and in the management of large multi-professional teams to Precision., avatar=Image{width=150,height=150,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/tiziana-magnani.webp',altText='',fileId=null}, linkedin=https://www.linkedin.com/in/tiziana-magnani-a9b288a, hs_name=, hs_path=, lastname=Magnani, hs_initial_published_at=1716212769184, hs_created_at=1709645745088, hs_is_edited=false, hs_deleted_at=0, name=Tiziana, job=, slug=tiziana-magnani, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: Decentralized trial strategies and their impact in rare disease studies Decentralized trial strategies and their impact in rare disease studies

    Clinical Trials - Rare Diseases

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778887, hs_child_table_id=0, hs_updated_at=1715690972359, hs_published_at=1738849393727, description=Andy Kinley, Ph.D. is Vice President of Innovation and Clinical Science at Precision for Medicine. He is a clinical researcher with over 25 years of combined experience leading basic and clinical research in oncology and hematology. His early scientific career focused on cancer cell signaling, setting a foundation to complement his clinical research roles in trial design and implementation of effective strategies for oncology clinical trials. Andy specializes in immuno-oncology trials (checkpoint inhibitors, T-cell agonists, bispecifics, cytokines, oncolytic viruses, neoantigen cancer vaccines), including autologous and allogeneic adoptive cell therapies (CAR-T, TCR, TIL, NK cells). Today, Andy identifies and implements innovative tools, datasets, and services that can impact clinical trial execution including quality, patient diversity, site identification, and trial timelines., avatar=Image{width=720,height=829,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/AndyKinley_headshot.png',altText='AndyKinley_headshot',fileId=167369936018}, linkedin=https://www.linkedin.com/in/andy-kinley-phd-5759551, hs_name=, hs_path=, lastname=Kinley, hs_initial_published_at=1716212769184, hs_created_at=1709645745118, hs_is_edited=false, hs_deleted_at=0, name=Andy, job=, slug=andy-kinley, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: When to Use CDISC Standards in Early Phase Clinical Trials When to Use CDISC Standards in Early Phase Clinical Trials

    Clinical Trials

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778853, hs_child_table_id=0, hs_updated_at=1709645745084, hs_published_at=1738849393727, description=Ryan Kurz is a Director of Statistical Programming with more than 20 years of experience supporting clinical trials., avatar=Image{width=150,height=150,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/ryan-kurz.webp',altText='',fileId=null}, linkedin=https://www.linkedin.com/in/ryan-kurz-b851b4173, hs_name=, hs_path=, lastname=Kurz, hs_initial_published_at=1716212769184, hs_created_at=1709645745084, hs_is_edited=false, hs_deleted_at=0, name=Ryan, job=, slug=ryan-kurz, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: Regulatory Risk Management Using Third-party Distributors Regulatory Risk Management Using Third-party Distributors

    Clinical Trials - Manufacturing - Regulatory

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778840, hs_child_table_id=0, hs_updated_at=1716132440837, hs_published_at=1738849393727, description=Maham Ansari, MS, RAC is a Senior Director, IVD Regulatory Affairs. Her focus is on companion diagnostic co-development programs, where she leverages her regulatory expertise to secure approvals in the US, Europe and beyond for companion diagnostics with a specific focus on gene therapy. She brings more than 16 years of global regulatory leadership experience in the medical device and in vitro diagnostics industry, spanning major multinationals to small start-ups, including full life cycle management across all stages of product development, execution of global regulatory strategies, and post-market surveillance.sh, avatar=Image{width=710,height=710,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Maham_Ansari.png',altText='Maham_Ansari',fileId=167373022876}, linkedin=https://www.linkedin.com/in/maham-ansari-ms-rac-6a735739, hs_name=, hs_path=, lastname=Ansari, hs_initial_published_at=1716212769184, hs_created_at=1709645745071, hs_is_edited=false, hs_deleted_at=0, name=Maham, job=, slug=maham-ansari, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: Inside a CRO: Growing Role of Medical Writers for an Effective CSR The Growing Role of Medical Writers for an Effective CSR

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778871, hs_child_table_id=0, hs_updated_at=1709645745102, hs_published_at=1738849393727, description=Meredith Latino is the Director of Medical Writing at Precision for Medicine. She earned a PhD in Molecular and Cellular Biology from Tulane University and brings more than 16 years of experience to the Precision team, including 9 years of medical writing and 8 years of academic research/writing., avatar=Image{width=150,height=150,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/meredith-latino.webp',altText='',fileId=null}, linkedin=https://www.linkedin.com/in/meredith-latino-7a2bba119/, hs_name=, hs_path=, lastname=Latino, hs_initial_published_at=1716212769184, hs_created_at=1709645745102, hs_is_edited=false, hs_deleted_at=0, name=Meredith, job=, slug=meredith-latino, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: Clinical Study Reports (CSR): Types and Use Cases Clinical Study Reports (CSR): Types and Use Cases

    Clinical Trials - Regulatory

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778871, hs_child_table_id=0, hs_updated_at=1709645745102, hs_published_at=1738849393727, description=Meredith Latino is the Director of Medical Writing at Precision for Medicine. She earned a PhD in Molecular and Cellular Biology from Tulane University and brings more than 16 years of experience to the Precision team, including 9 years of medical writing and 8 years of academic research/writing., avatar=Image{width=150,height=150,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/meredith-latino.webp',altText='',fileId=null}, linkedin=https://www.linkedin.com/in/meredith-latino-7a2bba119/, hs_name=, hs_path=, lastname=Latino, hs_initial_published_at=1716212769184, hs_created_at=1709645745102, hs_is_edited=false, hs_deleted_at=0, name=Meredith, job=, slug=meredith-latino, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: Phase I Clinical Trial Designs: Bayesian Optimal Interval Design (BOIN) Phase I Clinical Trial Designs: Bayesian Optimal Interval Design (BOIN)

    Clinical Trials - Early Phase Research - Oncology

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778861, hs_child_table_id=0, hs_updated_at=1716556164194, hs_published_at=1738849393727, description=Ed Matthews is a biostatistician with 26 years’ experience in medical statistics, having worked on multiple clinical studies, in a wide cross-section of therapeutic areas, focused on oncology, and in all clinical phases (I to IV). He is practiced in working on a variety of study requirements, including SAPs, electronic Case Report Forms (eCRFs), Clinical Study Reports (CSRs), protocols, clinical summaries and ISS/ISE, both in the UK, Europe and globally. Ed also has many years’ experience of PK analysis, in guiding and training both Statisticians and non-Statisticians, and experience with data safety boards as both an attendee and chair., avatar=Image{width=600,height=700,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Ed-Matthews.png',altText='Ed-Matthews',fileId=168384970145}, linkedin=https://www.linkedin.com/in/ed-matthews-919a4810, hs_name=, hs_path=, lastname=Matthews, hs_initial_published_at=1716213113382, hs_created_at=1709645745092, hs_is_edited=false, hs_deleted_at=0, name=Ed, job=Executive Director, Biostatistics, slug=ed-matthews, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: Rare Disease Clinical Trials in Pediatric Populations: Lessons Learned Rare Disease Clinical Trials in Pediatric Populations: Lessons Learned

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      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778849, hs_child_table_id=0, hs_updated_at=1714461239390, hs_published_at=1738849393727, description=Traci Fulton is Vice President of Project Management at Precision for Medicine, providing senior level oversight and support for clinical trials spanning rare disease, oncology and CNS indications. Ms. Fulton brings over 21 years’ experience with CRO teams, supporting the conduct of clinical trials across all phases, with over 18 years of her career focused on execution and delivery for complex clinical trials in oncology and rare diseases. She is passionate in her approach to support trials and her drive to support advancements in the treatment for underserved patient populations., avatar=Image{width=576,height=576,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Traci%20Fulton.webp',altText='Traci Fulton',fileId=165892782093}, linkedin=https://www.linkedin.com/in/traci-kruckemyer-fulton-70ab42a, hs_name=, hs_path=, lastname=Fulton, hs_initial_published_at=1716212769184, hs_created_at=1709645745080, hs_is_edited=false, hs_deleted_at=0, name=Traci, job=, slug=traci-fulton, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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  • Read: Why Satellites Sites are the Next Rising Stars in Clinical Research Why Satellites Sites are the Next Rising Stars in Clinical Research

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    Why Satellites Sites are the Next Rising Stars in Clinical Research

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      Rob Maiale

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