Clinical Trial Manager overseeing clinical trials managing operations and compliance in Brazil at IQVIA. Ensuring adherence to protocols and managing country - specific requirements.
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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