At Prime Services, we drive clinical trials forward with precision, planning, and proactive oversight. From startup to study close-out, our Clinical Operations team ensures your trials run efficiently, ethically, and on time—no matter the complexity.
We identify and activate high-performing investigative sites aligned with your protocol and goals. From site feasibility assessments to training, monitoring, and close-out, we ensure each site meets GCP and regulatory standards.
Every trial is led by a dedicated Project Manager backed by a skilled cross-functional team. We coordinate all moving parts—from site operations and data flow to vendor oversight—while applying risk-based and adaptive methodologies for smoother delivery.
We offer both remote and onsite monitoring to ensure protocol adherence, subject safety, and data accuracy. Our CRAs use real-time tools to spot and resolve issues proactively—keeping your trial on track.
We conduct internal regulatory audits and compliance checks to prepare your sites and study documentation for inspections—minimizing risk and maximizing confidence.
| Site Feasibility & Selection | Vendor Coordination |
| Study Startup & Initiation | Risk-Based Monitoring |
| Trial Master File (TMF) Management | Site Management |
| Investigator Meeting Support | Quality Management |
We deliver high-quality, compliant, and patient-centered clinical trials through expert planning, seamless execution, and risk-based oversight.
