See Beyond the Keyhole with RBQM Clinical Trials

Increase data integrity with our expert scientific and analytics data review teams

The Clinical Science & Centralized Monitoring experts at Precision redefines data integrity through a fusion of scientific expertise and cutting-edge analytics. Powered by our proprietary platform, Clinscope, we deliver a smarter, more agile approach to risk-based quality management—one that prioritizes what matters most: critical data, patient safety, and regulatory confidence.

Precision’s RBQM Clinical Trials Framework is Built for What’s Next

Streamline your clinical journey, enhance efficiency and accelerate your path to success with expert data integration, analysis, and interpretation.

Using an integrated model that shifts away from traditional monitoring, we replace exhaustive reviews with targeted, insight-rich analysis.

50+ pre-built dashboards tailored for rapid insight and therapeutic relevance
Clinscope-powered centralized monitoring detects outliers, trends, and site-level risks with precision
Therapeutic-specific standards (RECIST v1.1, iRECIST, IMWG, Lugano, etc.) ensure consistency and accuracy
Proprietary data visualization tools allow for highly focused strategic reviews, catching complex issues beyond programmed edits
Proactive tech-enabled alerts flag complex data quality issues before they escalate
Cross-functional collaboration across Medical, Biostats, Data Management, and Clinical Ops ensures holistic data integrity
Real-time analytics drive quality outcomes and support pivotal trial decisions

By leveraging therapeutic expertise and real-time data visualization, complex trial data transforms into actionable intelligence to accelerate timelines and empower smarter decisions across the study lifecycle.

20 Avg. years research experience

15 Avg. years oncology experience

20 Global team members

8 Avg. years with Precision

Lifecycle RBQM Support From Start-Up to Submission

Our Clinical Science & Centralized Monitoring team combines scientific rigor with scalable innovation. With decades of therapeutic experience and global reach, we apply risk-based quality management (RBQM) and centralized monitoring to ensure data fidelity from study start-up through database lock. Powered by Clinscope visualization tools and therapeutic-specific standards, every stage of your trial is guided by clarity, confidence, and control.

Start-Up

Start-Up

Aligning data capture with protocol and therapeutic standards

Our experts ensure the study design is built on a solid foundation for data precision.
Conduct

Conduct

Centralized, holistic, therapeutic data review

Dashboards and real-time analytics highlight site-level risks while expert reviewers identify issues standard checks miss.
Risk Mitigation

Risk Mitigation

Proactive alerts and cross-functional collaboration

Tech-enabled signals flag issues before they escalate, supported by Medical, Biostats, Data Management, and Clinical Ops teams.
Lock

Lock

On-time, confident database lock

Continuous centralized review streamlines final medical review and prepares submission-ready datasets.

Precision CSAI's Smart Patient Profiles clearly are the result of a lot of effort. They are certainly an extremely helpful tool to monitor patient data.

— Medical Director, Small Biotech
Precision's use of Smart Patient Profiles projects patient data to support informed decision-making. We have found them to be instrumental.

— Project Manager, Midsized Biotech
Precision is part of our team. They put in long days and hard work to help us create the slide deck that allowed our study to move forward. We are so appreciative of how fast they worked.

— Senior Manager, Clinical Trials, Midsized Biotech
Precision's use of Smart Patient Profiles projects patient data to support informed decision-making. We have found them to be instrumental.

— Project Manager, Midsized Biotech

Insights from Precision’s experts

Stay ahead with the latest insights from Precision’s team of experts. Discover valuable perspectives, updates, and strategies to navigate early and late phase development.

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Clinical Trials - Oncology

Case Study: Swift Stabilization in Phase 1 Solid Tumor Rescue

Jan 22, ‘26 | 10 min read

has not third author: true, (SizeLimitingPyMap: {main={hs_id=205683637283, hs_child_table_id=0, hs_updated_at=1769114822287, hs_published_at=1769114824037, 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=26433386}, second={hs_id=205683637278, hs_child_table_id=0, hs_updated_at=1769114711193, hs_published_at=1769114824037, 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=26433386}, third={}})

Karen S.
Annie R.

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Clinical Trials - Regulatory

The EU Biotech Act: What Sponsors Need to Know About Europe's Biotechnology Transformation

Jan 20, ‘26 | 17 min read

John McIntyre, PhD

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Clinical Trials - Oncology

Navigating Complexity: Rescuing a Biomarker-Driven Breast Cancer Trial

Jan 16, ‘26 | 4 min read

Alexis Hobbins-White

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Delivering Clinical Success Across Phases

Clinical Development Strategy

Unlock the full potential of your clinical trials with our tailored Clinical Development Strategies. Designed to navigate the complexities of trial execution, Precision can propel your program toward accelerated success.
Services Offered:
- Clinical Development Planning
- Clinical Trial Design
- Biomarker Trial Strategies
- Basket, Master & Umbrella trials
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Full-Service CRO

Experience seamless integration and meticulous management of your clinical trial with our Full-Service CRO. We ensure every detail is managed with expertise to drive your study towards its successful completion.
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

Amplify your clinical trial efficiency with Precision’s Functional Service Provider (FSP) solutions, offering specialized support focused on your project's unique needs.
Solutions Offered:
- FSP Clinical Monitoring
- FSP Drug Safety & Pharmacovigilance
- FSP Data Management
- FSP Biostatistics
- FSP Statistical Programming
- FSP Medical Writing
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Advance therapeutic breakthroughs with Precision

Explore the breadth of our expertise in therapeutics and modalities, as we lead your novel treatments in Oncology, Rare Diseases and beyond, from the groundbreaking idea to clinical realization.

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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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Award-winning CRO with deep oncology and rare disease expertise

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Exceptional translational and biomarker sciences with global central lab services

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