Review of Study Protocol, Informed Consent Form and CRF, for BA/ BE studies with a focus on providing medical inputs. 2. Monitoring and supervision of the clinical safety parameters (including clinical laboratory investigations) & management of adverse events during the conduct of studies. 3. Review of medical screening records (including clinical laboratory investigations) of the prospective subjects so as to ascertain their suitability for inclusion in clinical studies. 4. Ensuring the accuracy and correctness of clinical raw data, analyzing it and providing inputs for the preparation of clinical reports. 5. Liaising with the Institutional Ethics Committee for review of study Protocols and Informed Consent Forms, and for the submission of clinical reports/ clinical updates/ safety reports for all the completed studies. 6. Assisting in training and continuously updating the information and skills of the Phlebotomists, Nursing Supervisors and Medical Officers.
4 Lac To 7 Lac P.A.
Pharma / R&D / Biotech
0 - 3 Years
MBBS, Other Doctorate Degree
mbbs principal investigator laboratory investigation