02 Oct
|
Cliantha Research
|
Ahmedabad
02 Oct
Cliantha Research
Ahmedabad
Role & responsibilities
-
Efficiently planning and executing the logistics of all clinical studies.
- Responsible for overall conduct of the bioavailability bioequivalence clinical studies under supervision.
- Responsible for selection of the participants in the trial, safety of the subjects, operation of the clinic, communication with the sponsor, ethics committee and study team.
- Responsible for screening of the participants in the trial and monitor the day to day activities of the study team.
Job Location: Ahmedabad
Required Qualifications/ Experience:
- MBBS degree from a recognized institution
- Valid Medical Registration Certificate
- 1-2 years of experience in conducting and managing Bioavailability (BA) and Bioequivalence (BE) studies.
📌 Doctor (Ahmedabad)
🏢 Cliantha Research
📍 Ahmedabad