Clinical Research

Graduate degree in Science B.pharm, Life Sciences, Biotech, Zoology, Botany, etc. with PG Diploma in Clinical Research is mandatory with minimum 1 years’ experience in Clinical Trials is desirable.

Design and evaluate oncology clinical trial frameworks — including study protocols, patient enrollment strategies, and regulatory compliance considerations

B.Tech/ M.Sc./ M.Tech degree or two years PG Diploma in Clinical Research / Clinical Research Management / Regulatory Affairs / Life Sciences or related field from a recognized University

Responsible for one or several of the following: processing of Individual Case Safety Reports (ICSRs) from various sources, Literature search and review, signal detection and management, tracking regulatory information

MSc in Life Science / M.Pharm. PG Diploma in Clinical research is Mandatory Or Msc in Clinical research. Required IEC Co-ordinator, under, Institutional Ethics Committee

B.Sc. in Nursing / Life Sciences / Pharmacy / Biotechnology / Clinical Research or allied health sciences from a recognised university. JIPMER, Puducherry

M.Sc./ M.Pharm (PG Diploma in Clinical Research is mandatory)/ M.Sc. in Clinical Research/ MBBS/ BDS/ BAMS/ BHMS/ BUMS (PG Diploma in Clinical Research is Mandatory) or PharmD or Equivalent Qualification

Post Graduate Degree, including the integrated PG degree, in Life Sciences from a recognized university with atleast three years of post-qualification experience in a research lab.

Bachelors Degree in Life Sciences / Clinical Research / Clinical Data Management with minimum 03 years relevant experience. OR Post Graduate Degree in Clinical Research.