Job Description
1. Responsible for developing strategy for clinical research.2. Conduct KOL visits to collect scientific inputs during protocol development and planning.
3. Reviewing of protocols and other study related documents.
4. Seeking scientific advice from regulatory agency.
5. Interacting with regulatory agencies on queries.
6. Contributing into report of studies
7. Interacting with team to discuss the further development of product on the basis of results of trial.
8. Medical monitoring of clinical trial
9. Ensuring that clinical trails are conducted according to the protocol, GCP and applicable regulatory requirements
Contact Details
- Recruiter Name:Kamran Ahmad
- Email :kamran.ahmad@cipla.com
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