Clinical Research Coordinator II at University of South Florida responsible for coordinating clinical research activities and ensuring participant data quality. Serving as main contact for sponsors and patients for specific research protocols.
About the role
- Principal Clinical Scientist developing clinical strategies for regulatory approval in medical devices. Collaborating with clinical study teams and regulatory authorities in Abbott's Structural Heart division.
Responsibilities
- Develops, writes, or mentors others in creation of clinical strategy, risk management, or clinical evaluation planning for products and process changes, to gain regulatory approval for product release.
- Designs or mentors others in the design of clinical trials and studies in collaboration with internal stake holders including clinical project management, clinical operations.
- Serve as an active member of study teams and provide scientific support to justify trial design and ongoing scientific analysis during protocol development.
Requirements
- Advanced degree in the sciences, medicine, or similar discipline.
- 8+ years of related work experience with a solid understanding of specified functional area, or an equivalent combination of education and work experience.
- Demonstrated scientific writing ability.
Benefits
- Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
- An excellent retirement savings plan with a high employer contribution.
- Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
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