Senior Clinical Operations Lead – Site Monitoring
Listed on 2026-10-07
-
Science
Clinical Research, Healthcare Compliance
Pro Pharma is seeking a Clinical Operations professional to oversee investigator site management and monitoring activities across assigned studies. You will lead the clinical monitoring teams with the client and internal teams, ensuring adherence to study plans, SOPs, and GCP/ICH guidelines.
You will also develop training materials and monitor data quality through site visits. The role requires advanced CRA skills, team leadership, and strong communication.
As a Senior Clinical Operations Lead – Site Monitoring, you will play an important part at Pro Pharma in Raleigh, NC, United States.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior Clinical Operations Lead – Site Monitoring role in the description above.
We appreciate your interest in this position.
Join Pro Pharma and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).