The Sr Site Activation Manager leads and manages site activation and start-up activities for global clinical trials, ensuring milestones and timelines are met. The role oversees regulatory, ethics/IRB, and site activation submissions across multiple countries and regions and serves as the primary contact for site start-up activities with sponsors, sites, vendors, and cross-functional teams. The manager provides strategic guidance on country-specific regulatory requirements and start-up processes, tracks start-up metrics and activation performance, resolves issues, and mitigates risks that could affect study timelines. The position also supports and mentors junior team members, contributes to process improvements, ensures compliance with GCP, applicable regulations, and company SOPs, and collaborates with Project Management and Clinical Operations teams to support study execution. It involves managing multiple studies and priorities in a fast-paced global environment.
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Job Type
Full-time
Career Level
Senior
Education Level
No Education Listed