Posted:1 week ago|
Platform:
Work from Office
Full Time
Job Description 1. To Conduct clinical phase of the study as an investigator as per protocol, SOPs, applicable regulatory guidelines. 2. Assess eligibility of the volunteer for participating in the study 3. To review SOPs, Protocols , CRF, study reports and provide necessary inputs. 4. To supervise administration of IMP, informed consent process all study activities for BA BE studies. 5. To manage adverse event serious adverse events during course of the study. 6. To resolve queries raised by QA QC during clinical phase of study 7. To assist head Clinic in day to day technical administrative matters. Education Graduation in Medicine Work Experience 5-10 years of relevant experience
Lupin
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