Our services
At Compass Research Consulting, we bring the perspective of former Directors of Research who have walked in your shoes. We help sites strengthen operations, protect data integrity, and stay inspection-ready — so you can focus on conducting high-quality clinical trials.
Site operations and efficiency
Running a research site is demanding. We review your daily workflows, identify inefficiencies, and implement practical solutions that keep your team moving smoothly. From delegation and scheduling to documentation support, we help ensure operations are reliable and compliant.
Data integrity and quality oversight
Clean, accurate data is the foundation of every successful study. We provide source document reviews, data entry checks, and internal monitoring support to minimize queries and protocol deviations. Our goal is to help your site deliver sponsor-ready data the first time.
FDA and sponsor readiness
Preparing for audits and inspections can be stressful. We conduct mock audits, review essential regulatory binders, and build CAPA plans to close gaps before sponsors or the FDA find them. With Compass, your site will feel confident and prepared for any review.
Site assessment and advisory
Every site has strengths — and areas for growth. We perform a full evaluation of your site’s operations, staff, and compliance, then deliver clear recommendations and action plans. Think of it as a “wellness check” for your research program, tailored to your goals.
Study start-up support
Strong study start-up sets the tone for success. We assist with feasibility questionnaires, budget negotiations, and preparation for Site Initiation Visits (SIVs). Our support ensures your site is ready on day one — with staff, systems, and documents aligned for a smooth launch.
Get started
Tell us a little about your site, and we’ll be in touch.