North AmericaFull TimeHealthcare
Remotely
pharmacovigilanceoraclefdaichpimsemaadverse events
Job Description
📋 Description
- This position contributes to worldwide surveillance of clinical trial patient safety data and
- Support safety-related data assessment and ad-hoc safety reports for assigned studies.
- Collaborate with medical monitor to plan and execute study safety reviews.
- Provide safety overview to clinical teams and sites as needed.
- Review study protocols for appropriate safety language and safety sections of reports.
- Maintain audit readiness for study deliverables.
Back to all jobs