Life Sciences

Responsible for the drug surveillance program including the necessary follow-up, risk assessment, and relatedness to product on adverse reaction reports, oversight of safety in clinical trials and post marketing programs

Masters Degree in Public Health / Life Sciences / Clinical Research / Social Sciences / Epidemiology. All-India Institute of Medical Sciences

M.Sc. in Clinical research or life sciences and / or Pharm.D/ M.pharm and Minimum 03 to 04 years of experience working as a Coordinator in Clinical trials or investigated-initiated research projects at reputed medical institutes. JIPMER

Degree in Life sciences with 3-year experience in conducting clinical trials Or Post graduation in biological sciences with 1 year experience

Data entry of safety data onto adverse event database and tracking systems.Review of adverse events for completeness, accuracy and appropriateness for expedited reporting.

M.Pharm / M.S (Pharm) / M. Tech (Pharm) / M.Tech in Pharmaceutics / Pharmacology & Toxicology / Pharmacology / Pharmaceutical Chemistry / MSc (with NET) in Chemistry. DRL, Tezpur (DRDO)

B.Sc 4 years programme/ B.Pharma/ MBBS/ Integrated BS-MS.MSc/BE/B.Tech or equivalent degree with 55% marks and passing of NET/GATE test. RIMS

Masters degree in Biotechnology / Microbiology / Botany / Life sciences or related areas. OR B. Tech / BS or equivalent degree in any other relevant quantitative fields.

Candidates holding a Masters degree (with at least 55% marks) in in Natural Sciences / Agriculture / Life sciences / Plant biology / Botany are eligible to apply.