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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.

Oncology Explore Rare Diseases Explore Autoimmune Explore Gene Therapy Explore Cell Therapy Explore

  • 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.
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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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    Manufacturing Solutions

    Proven pioneer in planning, building and maintaining complex manufacturing facilities for biotech and large pharma.

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

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Clinical Trials

Case Study Phase 3 NSCLC: Site Relationships Streamline Feasibility

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    Anna Rodecki
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Clinical Trials

Source Data Verification Types, Trends, and Tips

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    has not third author: true, (SizeLimitingPyMap: {main={hs_id=183222587782, hs_child_table_id=0, hs_updated_at=1732630460690, hs_published_at=1739807653319, description=Jelena Alexander brings 18 years of industry experience across the CRO, biotech and R&D arenas, with the last eight years focused on clinical operations oversight and aligning resources with project needs. Prior to transitioning to clinical research, Jelena obtained a Master’s degree in infectious disease and immunology, specializing in the development of cross-reactive and neutralizing monoclonal antibodies to foot-and-moth disease virus. Jelena is a collaborative leader recognized for fostering relationships with stakeholders to embed sustainable workflow processes and for delivering high quality outputs to ensure business needs are accomplished on time and within budget. Jelena’s expertise extends to evaluating and assessing clinical proposals, with a focus on monitoring strategies, and operational feasibility. In this role, Jelena leverages operational and leadership expertise to deliver high-quality, client-focused solutions while enhancing efficiency and sustainability in proposal strategies. Jelena is devoted to driving innovation, mentoring teams, and achieving results through adaptability and commitment to quality., avatar=Image{width=800,height=800,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Jelena%20Alexander.jpg',altText='Jelena Alexander',fileId=183228271491}, lastname=Alexander, hs_initial_published_at=1732630470588, hs_created_by_user_id=26433386, hs_created_at=1732630317363, hs_is_edited=false, hs_deleted_at=0, name=Jelena, job=Senior Manager, Global Clinical Monitoring, slug=jelena-alexander, hs_updated_by_user_id=26433386}, second={}, third={}})
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    Jelena Alexander
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Read: How to launch a clinical trial in South Korea: Investigational New Drug Application Process How to launch a clinical trial in South Korea: Investigational New Drug Application Process

Clinical Trials - Regulatory

How to launch a clinical trial in South Korea: Investigational New Drug Application Process

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  • MeeHyun B. avatar

    MeeHyun B.
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    Helen O.
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