Design and evaluate oncology clinical trial frameworks — including study protocols, patient enrollment strategies, and regulatory compliance considerations
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.
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.
Perform site feasibility, identify potential investigator, negotiate study budget with potential investigators, finalization of investigators, sites, and execution of CDA and study-related contracts, Clinical Research Associate at Sun Pharma