Skip to content
Precision for Medicine
Upcoming Webinar

Breaking Barriers with PCR: Innovative Solutions for Clinical Trial Success

CRO-Hero européen

Precision European CRO Services

Développement intégré d'essais cliniques dans toute l'Europe, exécuté avec précision.
Avec les services de CRO européens de Precision, vous accédez aux avantages distincts d'un recrutement accéléré des patients, de sites bien équipés, d'investigateurs experts dévoués et de résultats de haute qualité. La vaste expérience de notre équipe à travers le continent ajoute la composante essentielle de l'expertise régionale pour améliorer vos stratégies cliniques globales.
L'Europe

Precision European CRO services - Une empreinte stratégique pour une exécution plus forte

En 2018, la position de Precision en tant que CRO mondial de premier plan avec une empreinte européenne robuste a été renforcée par l'acquisition d'Argint International, une CRO de premier plan spécialisée dans l'Europe centrale et du Sud-Est.

Notre présence stratégique en Hongrie, en Pologne, en Roumanie, en Slovaquie et en Serbie facilite l'accès à un bassin de patients diversifié, ce qui accélère le recrutement des patients. Cette présence, associée à un environnement de recherche clinique bien établi et à un écosystème réglementaire favorable, permet de rationaliser l'expérience des essais.

4. Vue de l'Italie depuis l'espace, de nuit (1)

Enraciné dans une expertise régionale approfondie, avec Precision

Avec les services d'essais cliniques, la science des données et les services de laboratoire spécialisés de Precision à travers l'Europe, nous offrons une expérience d'essai globale véritablement intégrée.

L'expertise de notre équipe régionale est inégalée en ce qui concerne la réalisation d'essais cliniques réussis en Europe. Cette équipe exceptionnelle de professionnels cliniques, de chefs de projet nationaux et de spécialistes de la réglementation connaît parfaitement le paysage réglementaire, clinique et culturel de la région et s'investit à fond dans votre programme clinique à chaque étape.

10 Bureaux dans toute l'Europe
700 Des experts au service de l'excellence clinique
4 Des laboratoires de précision pour un développement clinique intégré

L'équipe Precision, moteur de votre réussite en Europe

  • Clare Fourrier

    Clare Sarvary Fourrier

    Senior Vice President, Clinical Operations

  • Chris-Ingram

    Chris Ingram

    Executive Director, Regulatory Affairs, Europe

  • Katie-McGuire

    Katie McGuire

    Senior Vice President, Regulatory and Site Start-Up

  • Frances Murphy

    Frances Murphy

    Regional Vice President, Clinical Business Solutions, EU & APAC

Modèles de livraison agiles à l'échelle mondiale

L'empreinte mondiale de Precision est la pierre angulaire de notre agilité et de notre adaptabilité. Des modèles de livraison sur mesure pour votre programme, établissant l'équilibre parfait entre les équipes sur site et offshore pour une efficacité optimisée.

  • Explorer
    iStock-863497498

    Externalisation complète

    Gestion intégrée des essais cliniques visant à assurer une prestation efficace et accélérée depuis le lancement de l'étude jusqu'à sa soumission.
    Explorer

    Externalisation complète

    Gestion intégrée des essais cliniques visant à assurer une prestation efficace et accélérée depuis le lancement de l'étude jusqu'à sa soumission.
    Explorer
  • Explorer
    Modèle d'externalisation hybride de précision

    Précision FSP

    Renforcer la capacité de votre équipe interne avec des experts de précision, en fonction des besoins de l'étude, du projet et du programme.
    Explorer

    Précision FSP

    Renforcer la capacité de votre équipe interne avec des experts de précision, en fonction des besoins de l'étude, du projet et du programme.
    Explorer

Perspectives mondiales et régionales des experts de Precision

Gardez une longueur d'avance grâce aux dernières informations fournies par l'équipe d'experts de Precision. Découvrez des perspectives, des mises à jour et des stratégies précieuses pour mener à bien des essais cliniques en Europe.

Read: Clinical AI at Scale: Why Trust Matters More Than Speed Clinical AI at Scale: Why Trust Matters More Than Speed

Clinical Trials

Clinical AI at Scale: Why Trust Matters More Than Speed

|
    has third author: false, (SizeLimitingPyMap: {main={hs_id=219402396746, hs_child_table_id=0, hs_updated_at=1787057935787, hs_published_at=1787135938204, description=Zulfat Kapadia is a Statistical Programmer with a scientist's heart and a programmer's precision, bringing over 11 years of experience in clinical data analytics. She currently works as a Statistical Programmer at Precision for Medicine, focusing on clinical data transformations and safety analytics. She is a SAS-certified Statistical Programmer with strong expertise in CDISC standards (SDTM and ADaM), turning raw clinical data into clean, submission-ready datasets and TLFs (Tables, Listings, and Figures). Her journey began with an M.Sc. in Microbiology from Gujarat University, followed by years as a Research Associate, where she worked hands-on with method development, validation, and LC-MS/MS analysis in GLP-regulated labs, including navigating regulatory audits. She later moved into SAS programming at Cognizant, building the technical foundation for her current specialization. A resourceful team player, she continues expanding her expertise across clinical and pharmaceutical domain., avatar=Image{width=1024,height=1536,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Zulfat%20Headshot.jpg',altText='Zulfat Headshot',fileId=219402357006}, lastname=Kapadia, hs_initial_published_at=1786648737451, hs_created_by_user_id=65712240, hs_created_at=1786648684030, hs_is_edited=false, hs_deleted_at=0, name=Zulfat, job=Statistical Programmer, slug=zulfat-kapadia, hs_updated_by_user_id=92535535}, second={hs_id=219402396744, hs_child_table_id=0, hs_updated_at=1786648683717, hs_published_at=1787135938204, description=As Principal Statistical Programmer, Shakila plays a key role in leading statistical programming activities for clinical development programs at Precision for Medicine. She has extensive experience managing study deliverables, supporting regulatory submissions, implementing CDISC standards, and collaborating with cross-functional teams to ensure high-quality and compliant clinical data outputs. Prior to joining Precision for Medicine, she held programming roles at ICON and Quintiles, where she contributed to global clinical trials across Oncology, Cardiovascular, Vaccine, and Diabetes therapeutic areas. She has led the development and validation of SDTM, ADaM, TLFs, define.xml, and submission-ready datasets for major health authorities including the FDA, PMDA, and EMEA. Beyond her expertise in SAS programming and clinical data standards, Shakila is passionate about process improvement, automation, and mentoring teams. She has recently expanded her capabilities in Data Science, gaining practical experience in Python, Machine Learning, R, and Tableau, and is keen on leveraging modern analytics and AI-driven approaches to enhance clinical research solutions., avatar=Image{width=1024,height=1536,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Shakila%20J%20Headshot.png',altText='Shakila J Headshot',fileId=219402114740}, lastname=Jagadeesan , hs_initial_published_at=1786648737451, hs_created_by_user_id=65712240, hs_created_at=1786648634345, hs_is_edited=false, hs_deleted_at=0, name=Shakila, job=Principal Statistical Programmer , slug=Shakila-Jagadeesan, hs_updated_by_user_id=92535535}, third={hs_id=219402097154, hs_child_table_id=0, hs_updated_at=1786648633237, hs_published_at=1787135938204, description=As Senior Manager of Statistical Programming, Sugumaran brings a wealth of experience to his role at Precision for Medicine, since March 2021. Prior to Precision for Medicine, he was associated with ICON Clinical Research for over 10 years across various roles in statistical programming. He has been actively involved in leading large and complex submissions for a diverse client base including large biopharma, biotech, and CROs. In addition to building his expertise in statistical programming, data analytics, and data visualization, he is deeply passionate about developing talent and cutting-edge software solutions. He is also actively involved with several social causes and CSR activities. Sugumaran holds an MBA in Pharmaceutical Management and a Master's in Bioinformatics. He is also currently pursuing a PhD in Bioinformatics., avatar=Image{width=1024,height=1536,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Sugumaran%20headshot.png',altText='Sugumaran headshot',fileId=219402130472}, lastname=Muthuraj, hs_initial_published_at=1786648737451, hs_created_by_user_id=65712240, hs_created_at=1786647962706, hs_is_edited=false, hs_deleted_at=0, name=Sugumaran, job=Senior Manager, Statistical Programming , slug=Sugumaran-Muthuraj, hs_updated_by_user_id=92535535}})
  • Zulfat K. avatar Shakila J. avatar Sugumaran M. avatar
  • Zulfat K.

    Shakila J.

    Sugumaran M.

Découvrir
Read: Hidden Strategic Edge in Clinical Trials: Financial Project Management Hidden Strategic Edge in Clinical Trials: Financial Project Management

Clinical Trials

Hidden Strategic Edge in Clinical Trials: Financial Project Management

|
    has not third author: true, (SizeLimitingPyMap: {main={hs_id=218300089344, hs_child_table_id=0, hs_updated_at=1785358312044, hs_published_at=1787135938204, description=Global Finance leader with 35+ years of progressive experience and over two decades in the global CRO industry. Proven track record of building and developing high-performing teams, leading complex financial operations, and driving strategic initiatives that improve business performance and scalability. Deep expertise in financial planning and analysis, contract negotiation, budgeting and forecasting, process optimization, auditing, cash flow management, and credit and collections. Passionate about fostering collaboration across finance, operations, and executive leadership to deliver data-driven insights, strengthen governance, and enable informed decision-making both internally and for our Sponsors., avatar=Image{width=800,height=800,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/1576750031793.jpeg',altText='1576750031793',fileId=218305569797}, lastname=Kane, hs_initial_published_at=1785358316248, hs_created_by_user_id=65712240, hs_created_at=1785358281109, hs_is_edited=false, hs_deleted_at=0, name=Romy, job=Vice President, Operational Finance, slug=romy-kane, hs_updated_by_user_id=92535535}, second={}, third={}})
  • Romy Kane avatar

    Romy Kane

Découvrir
Read: Why Global Oncology Evidence May Not Support U.S. Regulatory Approval Why Global Oncology Evidence May Not Support U.S. Regulatory Approval

Clinical Trials - Regulatory

Why Global Oncology Evidence May Not Support U.S. Regulatory Approval

|
    has not third author: true, (SizeLimitingPyMap: {main={hs_id=167363064857, hs_child_table_id=0, hs_updated_at=1719905898183, hs_published_at=1787135938204, description=Industry-leading oncologist and demonstrated medical leader in precision medicine, novel trial design and innovative regulatory initiatives designed to expedite drug approvals. Draws on nearly a decade leading oncology and rare disease programs at the FDA. Former fellow at the National Cancer Institute and frequent featured speaker at ASCO and AACR. CDER technical authority on oncologic drug and biological products for thoracic and head and neck malignancies, neurologic tumors, pediatric solid tumors and rare tumors., avatar=Image{width=553,height=580,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Harpreet-Singh2.png',altText='Harpreet-Singh2',fileId=171747124346}, linkedin=https://www.linkedin.com/in/harpreetsinghmd/, team=[{id=163072475007, name='Precision for Medicine Leadership'}], lastname=Singh, MD, hs_initial_published_at=1715692570942, hs_created_by_user_id=2737751, hs_created_at=1715692477118, hs_is_edited=false, hs_deleted_at=0, name=Harpreet, job=Chief Medical Officer, slug=harpreet-singh, hs_updated_by_user_id=92535535}, second={}, third={}})
  • Harpreet Singh, MD avatar

    Harpreet Singh, MD

Découvrir

Des capacités spécialisées à chaque étape du développement clinique

Tirer parti d'une infrastructure intégrée qui réduit les inefficacités inhérentes à un développement complexe. Intégrer l'exécution des laboratoires et des essais pour accélérer la mise sur le marché. Precision peut personnaliser et faire converger ses capacités pour répondre aux besoins uniques de votre programme, ce qui favorise l'efficacité, l'agilité et la réussite du début à la fin.

  • Discover Explorer
    soutien aux essais cliniques

    CRO mondial
    Services

    CRO primé avec une grande expertise en oncologie et en maladies rares

    Explorer
  • Discover Explorer
    Services de laboratoire spécialisés

    Laboratoire mondial
    Services

    Des sciences translationnelles et des sciences des biomarqueurs exceptionnelles avec des services de laboratoire central à l'échelle mondiale

    Explorer
Clare Fourrier
Clare Sarvary Fourrier

Senior Vice President, Clinical Operations

Veteran of global oncology clinical operations, with in-depth experience in phase 1-3 oncology and hematology research as well as early-phase studies. Builder of world-class oncology research teams and leader of strategic growth of resources and operations across Europe. Keenly focused on study delivery, mitigation of study risk, and client service.

Chris-Ingram
Chris Ingram

Executive Director, Regulatory Affairs, Europe

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.

Katie-McGuire
Katie McGuire

Senior Vice President, Regulatory and Site Start-Up

Seasoned pharma leader with extensive expertise in oncology drug development and early phase clinical development. Veteran across multiple therapeutic indications in a wide range of multi-country, full-service studies through every phase. Strong communicator and trained executive coach who thrives on change and excels under pressure.

Frances Murphy
Frances Murphy

Regional Vice President, Clinical Business Solutions, EU & APAC

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.