About Us
Who We Are
At Partners Research Strategies, we specialize in optimizing clinical research sites through expert site management, regulatory compliance, and operational efficiency strategies. As a trusted Site Management Organization (SMO), we empower research sites to streamline workflows, improve recruitment, and secure more clinical trials.
Our Mission
Our mission is to transform research sites into high-performing, sponsor-preferred locations by ensuring efficiency, compliance, and strategic growth. Through tailored service plans, we help research sites reduce delays, increase enrollment, and maintain the highest regulatory standards.
What We Offer
🔹 Site Optimization & Process Improvement – SOP reviews, staff retraining, and workflow enhancements
🔹 Study Start-Up & Business Development – Contract negotiation, sponsor alignment, and regulatory submissions
🔹 Recruitment & Retention Strategies – Custom solutions to enhance participant enrollment and retention
🔹 Regulatory & FDA Compliance – IRB management, FDA audit preparation, and ongoing monitoring
🔹 Full-Service SMO Support – End-to-end site management, ensuring study success from initiation to completion
📞 Ready to take your research site to the next level? Contact PRS today!
At PRS, our team members bring over 27 years of extensive experience in clinical research, offering a unique blend of sponsor-side and site-side expertise. Our team has successfully navigated every phase of clinical trials, from site selection to study close-out, ensuring sites operate at peak efficiency while maintaining compliance.
✔ Expertise in managing studies for sponsors & CROs
✔ Proven success in optimizing operational site management
✔ Comprehensive support for clinical research sites at every stage
With a deep understanding of sponsor expectations and a track record of streamlining workflows, PRS equips research sites with the tools and strategies needed for sustained success in the industry.