A company is looking for an Associate Director, Site and Monitoring Health.
Key Responsibilities
Develop and oversee the Site and Monitoring Health strategy for clinical trials, ensuring alignment with ICH GCP standards
Lead and support Site and Monitoring Health Leads in evaluating CRO monitoring effectiveness across the portfolio
Manage day-to-day activities of FSP Vendor Site and Monitoring Health Leads and ensure compliance with oversight plans
Required Qualifications
Bachelor's Degree required; clinical or advanced degree preferred
Previous experience in Sponsor Oversight and Site and Monitoring Health preferred
Proven leadership experience with remote teams
Solid direct monitoring experience with a CRO or pharmaceutical company
Comprehensive knowledge of regulatory standards, including GCPs
Associate Director Of • Austin, Texas, United States