Supervising Clinical Operations Project Manager
$140,573–$183,826 year
On-site · San Diego, California, United States
Job Summary
Oversee a team of Project Managers and Coordinators to drive the successful execution of ATRI clinical trials across multiple national and international sites. Serve as the guidance expert for assigned studies, escalate issues, and collaborate with the Project Director and functional groups during planning and administration of all phases of multi-site trials. Set and maintain priorities and timelines for implementation, maintenance, and closeout; conduct study planning meetings; develop materials such as protocols, training manuals, source documents, and work instructions; create templates and guidelines aligned with regulations, SOPs, and SOP-based departmental initiatives; leverage excellent interpersonal skills to communicate with all levels of staff and stakeholders; and operationalize all clinical trial components.
Required Qualifications
- Five years of experience in clinical trials is required
- History of supervising staff
- On-site clinical trial monitoring experience
- Experience with ICH-GCP guidelines and SOPs
- Ability to develop study materials and manage study documents
- Strong written and verbal communication skills
- Ability to coordinate across multiple sites and vendors
- Education as specified: Associate's or Bachelor's degree (minimum)
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