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Clinical Trial Management Services

Execute your trials with Precision: Unrivaled Clinical Trial Management for global impact
Empower your clinical research with Precision for Medicine's bespoke Clinical Trial Management Services. Our approach seamlessly blends innovation in early-phase trials with robust effectiveness in late phases, ensuring your research advances confidently towards its goals. With an unwavering commitment to excellence, we propel the advancement of life-changing therapies for patients in need around the globe.

End-to-end Clinical Trial Management services

Precision for Medicine's end-to-end capabilities unite expert teams and global reach with advanced processes and technologies. By transforming complex data into actionable insights, we not only navigate the intricacies of each phase but also empower each trial with the agility and insight needed to drive success from concept to conclusion. Our strategic and collaborative approach to clinical trial management services accelerates trial success, setting new industry standards.

CRO Leadership Awards 2024

Award-winning clinical trial management services

Precision for Medicine's receipt of the 2024 CRO Leadership Awards in every category signifies more than our excellence; it highlights our partnership's value in propelling your clinical trials forward. Our award-winning expertise delivers not just superior trial management but a shared mission in bringing transformative therapies to patients globally.

See how our consistent recognition in the industry underscores our commitment to excellence in clinical trial management.

Explore our accolades
3500 Experts fueling innovation
600 Global trials driving progress
20 Years of clinical excellence

Advancing outcomes at every stage

  • Discover Early Phase Excellence
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    Early Phase Excellence

    Embark on the critical first steps of clinical discovery with our expertly managed early phase trials, where meticulous attention meets innovative strategy.

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  • Discover Late Phase Success
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    Late Phase Success

    Discover the path to market with our Late Phase Development expertise – delivering precision, compliance, and efficiency for your clinical journey.

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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

Specialized capabilities in every stage of clinical development

Leverage an integrated infrastructure that reduces the inefficiencies inherent in complex development. Integrate lab and trial execution to accelerate speed to market. Precision can customize and converge our capabilities to meet your program's unique needs—driving efficiency, agility, and success from start to finish.

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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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Read our latest Precision insights

Stay updated with the latest insights in statistical programming and automation through our blog. 

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Read: Phase I Clinical Trial Designs: Continuous Reassessment Method (CRM) Phase I Clinical Trial Designs: Continuous Reassessment Method (CRM)

Phase I Clinical Trial Designs: Continuous Reassessment Method (CRM)

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  • Kurt Preugschat avatar

    Kurt Preugschat
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Read: Phase I Clinical Trial Designs: Bayesian Logistic Regression Model (BLRM) Phase I Clinical Trial Designs: Bayesian Logistic Regression Model (BLRM)

Phase I Clinical Trial Designs: Bayesian Logistic Regression Model (BLRM)

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  • Kurt Preugschat avatar

    Kurt Preugschat
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Read: Why 100% SDV Is No Longer Feasible — and How Risk-Based Monitoring Saves Time, Money, and Your Trial Why 100% SDV Is No Longer Feasible — and How Risk-Based Monitoring Saves Time, Money, and Your Trial

Clinical Trials

Why 100% SDV Is No Longer Feasible — and How Risk-Based Monitoring Saves Time, Money, and Your Trial

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    has not third author: true, (SizeLimitingPyMap: {main={hs_id=187570680222, hs_child_table_id=0, hs_updated_at=1742413198455, hs_published_at=1748379090824, description=Christine has been ensuring high performance delivery of clinical research projects for more than 23 years. During this time, she has successfully led diverse teams across various cancer indications including renal, pancreatic, melanoma, lung, head and neck, breast, multiple myeloma, extra-nodal NK/T lymphoma, non-Hodgkin’s lymphoma, and Hodgkin’s lymphoma. Within the CRO setting she also supported the strategic development of over 50 hematology/oncology programs including complex Phase 1 projects in immuno-oncology and autologous cell therapy. She also led the establishment of a novel oncology research infrastructure which accelerated study activations for Phase 1 solid tumor studies. Christine obtained her master’s degree in public health at the University of Texas where she also trained in the development and implementation of clinical and epidemiologic research at the Coordinating Center for Clinical Trials as well as the Center for Occupational and Environment Health., avatar=Image{width=1200,height=1200,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Christine%20Lusk-1.png',altText='Christine Lusk-1',fileId=187579105870}, lastname=Lusk, hs_initial_published_at=1742410730688, hs_created_by_user_id=26433386, hs_created_at=1742410650472, hs_is_edited=false, hs_deleted_at=0, name=Christine, job=Director, Project Management, slug=christine-lusk, hs_updated_by_user_id=51739740}, second={hs_id=190691157084, hs_child_table_id=0, hs_updated_at=1748379058655, hs_published_at=1748379090824, description=Over the last 15 years, Megan has played a key role in advancing multiple oncology compounds through various stages of development, across numerous tumor types. Having worked at both biotech and CRO companies, Megan brings a comprehensive understanding of clinical operations and drug development. Megan maintains a focus on accelerating the development of innovative cancer therapies to improve patient outcomes worldwide., avatar=Image{width=3024,height=4032,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Megan%20Knoch.jpg',altText='Megan Knoch',fileId=190688034156}, lastname=Knoch, hs_initial_published_at=1748379090824, hs_created_by_user_id=26433386, hs_created_at=1748379018316, hs_is_edited=false, hs_deleted_at=0, name=Megan, slug=megan-knoch, hs_updated_by_user_id=26433386}, third={}})
  • Christine L. avatar

    Christine L.
  • Megan K. avatar

    Megan K.
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