Rapid Study
Start-up and
Feasibility Assessment

With an established global network of clinical trial “Centers of Excellence” and efficient study start-up processes that provide the flexibility needed during this crucial period, Precision moves your project from protocol to first-patient-dosed quickly and reliably.

Getting clinical trials off the ground fast

Tight team integration and clear two-way communications ensure study start-up success
We’ve turned clinical trial study start-up into a science
  • We ensure close coordination and alignment of key site representatives with all parties involved
  • We provide detailed documentation and training for all aspects of the study
  • We include separate manuals specifically for pharmacy, radiology, laboratory, and drug administration
So you can stay focused on the science coming out of your clinical trial
  • Access global key opinion leaders in your specific indication
  • Receive updates and answers whenever you need them
  • Have the confidence of knowing that seasoned professionals with years of experience are dedicated to your project

Case Study: Targeted strategies secure enrollment for a phase 2 trial for eosinophilic esophagitis 2 months ahead of schedule

Precision was asked to manage enrollment for a double-blind, placebo-controlled phase 2 trial. The study sought to enroll 100 adult patients with biopsy-confirmed eosinophilic esophagitis at 40 centers across the United States, but Precision had to overcome 3 key hurdles:

  • The initial trial design included both pediatric and adult patients; following FDA feedback, the protocol was redesigned as an adult-only trial. This further limited the potential patient pool of this rare disease trial
  • Site feedback identified an enrollment criterion that represented a potentially significant barrier to patient recruitment
  • The sponsor requested the anticipated 12-month enrollment time frame to be accelerated in an effort to get topline results earlier.

Find out how Precision met the enrollment goals 2 months ahead of schedule by reading the complete Case Study.

Tell us about your project requirements

Whether this is the first clinical trial study you’re involved in or the twenty-first, we have the experience and agility to meet your needs. Let us know how we can help.

Tell us about your project requirements

Whether this is the first clinical trial study you’re involved in or the twenty-first, we have the experience and agility to meet your needs. Let us know how we can help.

Clinical trial services

Global Clinical Trial Footprint

Sample processing labs, clinical trial sites and offices in five continents provide the clinical reach and scale to manage complex global programs.

Clinical Development Strategy

Tailored strategies consider the scientific, regulatory, and commercial factors that shape each trial, mitigating risk and advancing the development pathway.

Clinical Trial Design

Advanced trial-design approaches—including basket, umbrella, and adaptive trials—deliver biomarker driven clinical research. Deep experience in these highly complex trial designs maximizes both insights and efficiency.

Biostatistics

Seasoned biostatisticians and statistical programmers deliver insight into every trial phase, from study design to regulatory submissions, all backed by meticulous documentation and data monitoring.

Clinical Sample Management

Sample inventories from a global network of labs supply real-time processing in 55 countries; consolidated data from central labs, screening labs, and specialty labs with clinical data create actionable reports.

Data Sciences

Get better visibility, better decisions, and better clinical execution with Precision’s data-first approach. Deep subject matter expertise and innovative analytics empower your critical clinical development milestones.

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