Full Service Clinical Research
One Partner Across Study Design, Start Up, and Execution, from Milestone to Milestone
Comprehensive, End-to-End Support for Your Complex Clinical Trials
At Premier Research, our focus is on empowering companies to advance innovative treatments with speed, agility, and scientific expertise. Our full-service clinical development model is designed to meet the complex needs of today’s dynamic regulatory and therapeutic landscape, offering a streamlined, technology-powered approach to study execution that delivers scientific rigor, operational efficiency, and strategic insight under one cohesive umbrella.
With more than 30 years of experience supporting complex, high-stakes trials, we partner with sponsors to navigate the intricacies of clinical trial design, patient recruitment, data integrity, and regulatory compliance. We align our capabilities with your program goals to reduce risk, accelerate timelines, and optimize outcomes.
From protocol development and clinical operations to regulatory strategy and pharmacovigilance, our teams bring therapeutic expertise, deep operational experience, and a commitment to quality that ensures your study is not only executed efficiently but also positioned for long-term value creation.
Study Design
Using a systematic strategy to minimize the time to key milestones and maximize the value of your investigational products, we unite your team and ours with a focus on your molecule, established endpoints, and the patient community, working toward a successful trial outcome.

Study Start Up
We bring together an experienced global team, proven processes, and innovative technologies to deliver smart study start up. Backed by technology and data, your trials meet timelines reliably and efficiently.

Medical Affairs
Our medical affairs professionals collaborate closely with your team, taking a cross-functional approach grounded in medical insight and backed by years of operational excellence.

Biostatistics & Data Management
Our experts deliver superior biostatistical and data management services for unmatched data delivery. We prioritize the seamless flow of quality data from study design through submission.

Central Monitoring
We deliver a fit-for-purpose central monitoring strategy that reduces risk, enhances patient safety, and optimizes resources in clinical trials. Real-time data review enables insights into site performance, streamlining oversight and improving efficiency.

Clinical Monitoring & Site Management
We offer comprehensive clinical monitoring services, encompassing both on-site and centralized monitoring for clinical trials. Our expertise in site management covers site selection, initiation, monitoring, and close-out, to ensure smooth execution for your studies.

Project & Risk Management
Our robust project and risk management processes are designed to identify and mitigate potential risks throughout the clinical trial lifecycle. We emphasize proactive risk identification and mitigation, streamlining operational workflows, and maintaining adherence to industry guidelines.

Safety & Pharmacovigilance
Our consultants and specialists design drug/device safety and pharmacovigilance services to fit your program’s demanding requirements. We manage the clinical safety process supported by a comprehensive framework of standard operating procedures (SOPs) and study-specific safety plans.

Quality & Compliance
We ensure that your clinical trials meet the highest standards of safety, quality, and compliance at every step, leveraging our expertise in international regulatory guidelines and all areas of good practices (GxPs) to minimize risks and optimize outcomes.

Medical Writing
Our dedicated medical writers work as a true extension of your team, seamlessly integrating to deliver high-quality, compliant documents. By bringing exceptional levels of clarity to your regulatory submissions, we can help accelerate the approval process and prevent costly delays.

Global Records Management
Our team provides comprehensive Trial Master File (TMF) services using a turnkey approach designed to fit the needs of your clinical program, backed by our global TMF Standard Operating Procedures and the CDISC TMF Reference Model.

Virtual Clinical Trial Services
Virtual clinical trials represent a significant advancement in clinical research methodologies. We help you design virtual trials and implement remote monitoring to broaden patient demographics, enhance trial diversity, and simplify long-term follow-up,

Agility and knowledge at your fingertips
Resources

9 Tips for Designing and Operationalizing Early-Stage Precision Oncology Studies

What Can a Corn Analogy Teach Us About Smarter Trial Oversight?

8 New Elements of the IVDR — and How to Change Your Approach
resources
Stay ahead of the curve by browsing our extensive library of white papers, case studies, blog posts, and more.