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Global CRO Services

Global reach, local precision: Comprehensive solutions to power your clinical trials worldwide.
At Precision for Medicine, we merge global reach with local insight to navigate the complexities of clinical trials with unparalleled expertise and precision. From full-service study execution to functional service solutions, our global scale and tailored strategies are crafted to enhance every phase of your clinical trial journey.

Global scale with Precision Clinical Trial Services

Precision for Medicine offers unmatched global clinical trial services, harnessing our extensive international presence to meet the comprehensive needs of your research. With expertise in over 50 countries, our local specialists provide invaluable insights and regulatory compliance, ensuring seamless execution across borders. Our global scale, combined with precise local knowledge, accelerates the progress of your clinical trials with efficiency and expertise.

Clinical Reach

Comprehensive clinical trial support: From strategy to execution

  • Clinical Development Strategy

    Unlock the full potential of your clinical trials with our bespoke Clinical Development Strategy, designed to navigate complexities and accelerate success.
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    Services Offered:


    • Clinical Development Planning
    • Clinical Trial Design
    • Biomarker Trial Strategies
    • Basket, Master & Umbrella trials
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  • Full-Service CRO

    Experience the seamless integration of comprehensive trial management with our Full-Service CRO, where every detail is expertly managed to drive your study's success.
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    Services include, but are not limited to:


    • Full-service Study Management
    • Study Start-up & Feasibility
    • Clinical Monitoring
    • Medical Monitoring
    • Drug Safety & Pharmacovigilance
    • Data Management
    • Biostatistics
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  • Precision FSP

    Enhance your clinical trial's efficiency with Precision’s Functional Service Provider (FSP) solutions, offering specialized support tailored to your project's unique needs.
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    Solutions Offered:


    • FSP Data Management
    • FSP Biostatistics
    • FSP Statistical Programming
    • FSP Medical Writing
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Deep experience with debilitating disease and unique modalities

Like you, we understand that there’s a patient throughout the development pathway. Supporting our partners to bring innovative treatments to patients is our purpose. Leverage our experience in these therapeutic areas.

  • Delivering Excellence in The Americas, Europe, and APAC

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    The Americas CRO

    Harnessing the diverse clinical landscape of The Americas to deliver research excellence and transformative health solutions.
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    Europe CRO

    Leveraging Europe's advanced healthcare systems to conduct sophisticated and efficient clinical trials.
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    APAC CRO

    In APAC, our trials tap into cutting-edge technology and vast patient populations to drive global health progress.

Specialized capabilities in every stage of clinical development

An integrated infrastructure that reduces the inefficiencies inherent in complex development

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    Global CRO Services

    A recognized leader in oncology and rare diseases with rich experience in complex trials

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    Laboratory
    Services

    Experts in translational and biomarker sciences with worldwide specialty labs and central lab services that are enabling breakthroughs.

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Discover actionable insights from thought leaders on the front lines of research.

Read: The Amendment Trap: Why 76% of Clinical Trials Face Six-Figure Protocol Changes The Amendment Trap: Why 76% of Clinical Trials Face Six-Figure Protocol Changes

Clinical Trials

The Amendment Trap: Why 76% of Clinical Trials Face Six-Figure Protocol Changes

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  • Christine Lusk avatar

    Christine Lusk

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Read: Best Practices to Streamline Development of Safety Update Reports (DSURs) Best Practices to Streamline Development of Safety Update Reports (DSURs)

Clinical Trials

Best Practices to Streamline Development of Safety Update Reports (DSURs)

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    has not third author: true, (SizeLimitingPyMap: {main={hs_id=182849803084, hs_child_table_id=0, hs_updated_at=1731697230236, hs_published_at=1742413203456, description=Lena Randhawa, PhD is a Principal Medical Writer at Precision for Medicine. She brings to Precision >23 years of written and oral communication experience and >12 years of regulatory medical writing experience, project management, and leadership roles. Lena has extensive experience across various regulatory documents including CSRs (interim CSRs, CSR amendments/addenda, and abbreviated/synoptic CSRs), CSR patient narratives, DSURs/IND annual reports, IBs and updates, clinical protocols and amendments, informed consent forms, IND/NDA components, and briefing packages., avatar=Image{width=1200,height=1200,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Lena%20Randhawa-1.jpg',altText='Lena Randhawa-1',fileId=182849417502}, lastname=Randhawa, hs_initial_published_at=1731697233687, hs_created_by_user_id=26433386, hs_created_at=1731697009126, hs_is_edited=false, hs_deleted_at=0, name=Lena, job=Senior Manager, Medical Writing, slug=lena-randhawa, hs_updated_by_user_id=26433386}, second={}, third={}})
  • Lena Randhawa avatar

    Lena Randhawa

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Read: Webinar Insights: Optimizing Cohort Management in Early-Phase Oncology Trials Webinar Insights: Optimizing Cohort Management in Early-Phase Oncology Trials

Clinical Trials - Oncology

Webinar Insights: Optimizing Cohort Management in Early-Phase Oncology Trials

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  • Rob M. avatar

    Rob M.

  • Niveda R. avatar

    Niveda R.

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