Clinical Trials Administrator Level 4
- Proactively identify funding and support opportunities for clinical research and education initiatives.
- Track opportunities and maintain timely correspondence with stakeholders.
- Assist researchers in developing proposals, protocols, and project materials for sponsor submission.
- Coordinate communication with sponsors and collaborators.
- Plan and participate in site feasibility activities to ensure deadlines and requirements are met.
- Collaborate with researchers, directors, and staff to develop study protocols, project management tools, and staffing plans.
- Support program operations by coordinating among stakeholders and monitoring progress.
- Organize and attend meetings with researchers, program directors, staff, sponsors, and collaborators.
- Prepare meeting materials, maintain notes, and track action items to ensure follow-up.
- Serve as a key liaison between leadership and research teams, ensuring smooth execution of program goals.
- Provide expert guidance on program operations, compliance, and documentation.
- A minimum of a bachelor’s degree
- Minimum of nine (9) years of professional experience in clinical research administration or a related field
- Deep understanding of clinical research operations, protocols, and regulatory requirements
- Strong organizational and project management skills
- Favorable background check
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