About the Job
Key responsibilities:1. Assist in the design, setup, and monitoring of clinical trials.
2. Communicate effectively with clinical investigators and trial site staff.
3. Conduct site visits to monitor clinical trial progress.
4. Ensure compliance with protocols, good clinical practice (GCP), and regulatory requirements.
5. Support the resolution of queries and discrepancies in clinical data.
Number of Openings
6 openingsPerks of this Jobs
5 days a week
Skills
Pharmacovigilance
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