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The Precision Blog
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Read Developing a Comprehensive Strategy for Implementing AI & Multi-Omics for Translational Research
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Read Back to the Source: A Translational Leader on Extending the Living Legacy of Genomic Data Back to the Source: A Translational Leader on Extending the Living Legacy of Genomic Data
Read The Collaborative Partnership Model: Your Team Amplified The Collaborative Partnership Model: Your Team Amplified
Read Empowering Clinical Operations with Enhanced Biospecimen Lifecycle Management Empowering Clinical Operations with Enhanced Biospecimen Lifecycle Management
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Read: The Collaborative Partnership Model: Your Team Amplified 
The Collaborative Partnership Model: Your Team Amplified
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Read: EMA PRIME Scheme Explained: Eligibility, Benefits, Risks, and When to Apply 
EMA PRIME Scheme Explained: Eligibility, Benefits, Risks, and When to Apply
has not third author: true, (SizeLimitingPyMap: {main={hs_id=195804116748, hs_child_table_id=0, hs_updated_at=1764696930757, hs_published_at=1770252999853, description=John is an experienced regulatory affairs consultant with more than 15 years of professional experience in drug development. He brings a proven track record in providing regulatory strategy, regulatory document development and review, and liaising with regulatory authorities., avatar=Image{width=276,height=290,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/John%20McIntyre.png',altText='John McIntyre',fileId=201584594055}, lastname=McIntyre, PhD, hs_initial_published_at=1757516163742, hs_created_by_user_id=26433386, hs_created_at=1757515873736, hs_is_edited=false, hs_deleted_at=0, name=John, job=Senior Director, Regulatory Strategy, slug=john-mcintyre, hs_updated_by_user_id=51739740}, second={hs_id=159488778852, hs_child_table_id=0, hs_updated_at=1765558855468, hs_published_at=1770252999853, 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=1200,height=1200,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Chris-Ingram.png',altText='Chris-Ingram',fileId=202456722303}, linkedin=https://www.linkedin.com/in/chris-ingram-0255b216, hs_name=, hs_path=, lastname=Ingram, hs_initial_published_at=1769114824102, 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=51739740}, third={}}) -
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Read: Case Study: Swift Stabilization in Phase 1 Solid Tumor Rescue 
Case Study: Swift Stabilization in Phase 1 Solid Tumor Rescue
has not third author: true, (SizeLimitingPyMap: {main={hs_id=205683637283, hs_child_table_id=0, hs_updated_at=1769114822287, hs_published_at=1770252999853, description=Karen Stokes is a dedicated, collaborative and solution-oriented drug development professional with over 25 years of experience in Data Management, Clinical Operations and Project Management on Phase I-IV studies in Academic and Contract Research Organization (CRO) environments. She has expertise in CNS, Rare and Oncology indications and have successfully led cross functional teams to deliver quality on time. , avatar=Image{width=208,height=246,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Karen%20Stokes.png',altText='Karen Stokes',fileId=205695655336}, lastname=Stokes, hs_initial_published_at=1769114824037, hs_created_by_user_id=26433386, hs_created_at=1769114779691, hs_is_edited=false, hs_deleted_at=0, name=Karen, job=Project Director, slug=karen-stokes, hs_updated_by_user_id=51739740}, second={hs_id=205683637278, hs_child_table_id=0, hs_updated_at=1769114711193, hs_published_at=1770252999853, description=Annie Raymond-Desgagné is a Principal Clinical Trial Manager specializing in oncology, known for her strong leadership, structured planning, and proactive mindset. She excels at building high‑performing teams, with a passion for mentoring and helping colleagues bring out the best in themselves. Skilled at implementing tools that improve forecasting and operational readiness, Annie consistently keeps teams two steps ahead in fast‑moving clinical environments. She has a particular affinity for first‑in‑human (FIH) studies, where the science unfolds in real time—an area that fuels her love of challenge and innovation. Collaborative, committed, and science‑driven, she brings clarity, foresight, and positive energy to every project she leads., avatar=Image{width=226,height=226,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/A%20person%20with%20short%20brown%20hair%20wearing%20glasses%20Description%20automatically%20generated.png',altText='A person with short brown hair wearing glasses Description automatically generated',fileId=205695412385}, lastname=Raymond-Desgagné, hs_initial_published_at=1769114715920, hs_created_by_user_id=26433386, hs_created_at=1769114644600, hs_is_edited=false, hs_deleted_at=0, name=Annie, job=Principal Clinical Trial Manager, slug=annie-raymond-desgagne, hs_updated_by_user_id=51739740}, third={}}) -
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Read: Developing a Comprehensive Strategy for Implementing AI & Multi-Omics for Translational Research 
Developing a Comprehensive Strategy for Implementing AI & Multi-Omics for Translational Research
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Read: Back to the Source: A Translational Leader on Extending the Living Legacy of Genomic Data 
Back to the Source: A Translational Leader on Extending the Living Legacy of Genomic Data
has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778886, hs_child_table_id=0, hs_updated_at=1763657611624, hs_published_at=1770252999853, description=Robert Snyder, PhD, is a seasoned expert with a 20-year track record in genomics, specializing in in vitro diagnostic assay development and bioinformatics. Committed to advancing medical science, he is proficient in regulatory V&V study designs and understands the nuances of orthogonal methods. A collaborative partner in biomedical development, Dr. Snyder champions the critical transition of biospecimens from benchtop to bedside., avatar=Image{width=576,height=576,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Robert%20Snyder.webp',altText='Robert Snyder',fileId=165892444501}, linkedin=https://www.linkedin.com/in/robert-snyder-ph-d-9b67b035, hs_name=, hs_path=, lastname=Snyder, PhD, hs_initial_published_at=1769114824102, hs_created_at=1709645745117, hs_is_edited=false, hs_deleted_at=0, name=Robert, job=, slug=robert-snyder, email=, hs_updated_by_user_id=51739740}, second={hs_id=164691024166, hs_child_table_id=0, hs_updated_at=1716326265678, hs_published_at=1770252999853, description=Respected veteran of the biospecimen and biomarker laboratory services industry. Honed his expertise through leadership roles in organizations including Roche, Cancer Genetics, and BioServe. Holds a Master of Public Health and a Masters of Business Administration from the Johns Hopkins University., avatar=Image{width=576,height=576,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Rob%20Fannon%20Headshot.webp',altText='Rob Fannon Headshot',fileId=165893006477}, linkedin=https://www.linkedin.com/in/rob-fannon-901378/, team=[{id=163072475009, name='Translational Sciences Leadership'}], lastname=Fannon, MPH, MBA, hs_initial_published_at=1713346931329, hs_created_by_user_id=62155952, hs_created_at=1713345787919, hs_is_edited=false, hs_deleted_at=0, name=Rob, job=General Manager, Biospecimen Solutions, slug=rob-fannon, hs_updated_by_user_id=51739740}, third={}}) -
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Read: Reflect on 20 Years of Cancer Research with MIRROR Biospecimens 
Reflect on 20 Years of Cancer Research with MIRROR Biospecimens
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All articles
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Read: Advancing Diversity in Oncology Clinical Trials: 5 Key Insights from Clinical Trial Sites 
Advancing Diversity in Oncology Clinical Trials: 5 Key Insights from Clinical Trial Sites
has not third author: true, (SizeLimitingPyMap: {main={hs_id=184750975030, hs_child_table_id=0, hs_updated_at=1754641219433, hs_published_at=1770252999853, description=Melanie Morris brings over two decades of experience in pivotal roles supporting Phase I to IV clinical trials within Site, CRO and Sponsor organizations. As Associate Director of the Precision Site Network at Precision for Medicine, Melanie is dedicated to fostering collaborative, mutually beneficial partnerships with clinical research sites, transforming transactional relationships into enduring alliances that drive shared success. With a career spanning leadership in clinical operations, functional service provider models, and decentralized trial execution, Melanie has consistently delivered innovative strategies that enhance site engagement and operational excellence. Passionate about creating impactful collaborations, Melanie aims to advance the clinical research landscape and support the development and acceleration of life-changing rare disease and oncology therapies., avatar=Image{width=287,height=287,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/Melanie-Morris-1.png',altText='Melanie-Morris-1',fileId=194123711868}, lastname=Morris, hs_initial_published_at=1736540185270, hs_created_by_user_id=26433386, hs_created_at=1736527212397, hs_is_edited=false, hs_deleted_at=0, name=Melanie, job=Associate Director, Precision Site Network, slug=melanie-morris, hs_updated_by_user_id=51739740}, second={hs_id=178046423372, hs_child_table_id=0, hs_updated_at=1754641388766, hs_published_at=1770252999853, description=Rosamund (Roz) Round is a seasoned expert in patient engagement and innovation bringing over 20 years of experience. She is focused on listening to and learning from patients and care partners to understand how to better improve trial access and experience. Roz successfully built and led decentralized clinical trials service through the pandemic and is now addressing the implementation of AI across various aspects of clinical research. She has a strong focus on diversity, equity, and inclusion (DEI) to drive health equity in clinical research. Roz holds an MSc in Health Psychology, studied Psychology and Immunology at Harvard University, and is a recognized thought leader with an extensive portfolio of publications, conference presentations, webinars, and vlogs., avatar=Image{width=287,height=287,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/Round-Rosamund.png',altText='Round-Rosamund',fileId=194123714174}, lastname=Round, hs_initial_published_at=1725972637852, hs_created_by_user_id=51739740, hs_created_at=1725972446462, hs_is_edited=false, hs_deleted_at=0, name=Rosamund, job=Vice President, PAtient Engagement & Innovation, slug=rosamund-round, hs_updated_by_user_id=51739740}, third={}}) -
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