Clinical Pharmacologist at Nizam's Institute of Medical Sciences
Industry
Medical / Health Care / Pharmaceuticals
About
Execution of clinical studies as a Principal Investigator as per regulatory requirements.
ICH-GCP Training.
Design and review of protocol, SOP, CSR, ICF and CRF and aiding in the design of research study
Reporting of adverse events/ADRs to PvPI National Coordinating Centre (PvPI NCC) through Vigiflow with the source data (original) attached with each ADR case.
Dose recommendations to clinicians (special population - Pediatric, geriatric, renal failure and hepatic failure patients).
Writing and developing study reports and journal articles collaboratively.
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