Principal Investigator(Ba/be Studies)
6 days ago
The investigator shall be responsible for the conduct of the trial according to the protocol and the Good Clinical Practices Guidelines, Ethical guidelines and Standard operating procedures.
- The investigator is responsible for reviewing, and approving the protocol, prior to the ethics committee approval.
- Consenting of Volunteers.
- Training and delegating of all study personal
- Seeking approvals from ethics committee for the clinical trials.
- To perform those trial-related duties and functions and should implement procedures to ensure the integrity of the trial-related duties and functions performed and any data generated.
- To ensure the confidentiality of the trial participants.
- To ensure that AEs and SAEs are adequately followed up, reported and documented and reporting to EC and DCGI if applicable.
- Qualifications
- MBBS/MD Pharmacology
- Should have at least 2-3 yrs experience in CRO as PI.
**Job Types**: Full-time, Regular / Permanent
**Benefits**:
- Health insurance
- Leave encashment
- Provident Fund
Schedule:
- Day shift
- Morning shift
**Speak with the employer**
+91 9030030162
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