Clinical Research

BSc. Life Science / B.Pharm with Post Graduate Diploma in Clinical Research (PGDCR). The activities include assisting PI/Co-I with screening of trial participants, documentation of IC process, ensuring Protocol compliance, IEC communication, data management, maintaining Investigator Study File, processing of participant reimbursements maintenance of study related trackers/ logs etc.

Postgraduate degree in a Life Sciences / Health Sciences / Public Health / Clinical Research with post-qualification experience OR PhD. clinical research/RCT coordination, GCP, data management, regulatory documentation and transplant/infectious-diseases research 

First Class Post Graduate Degree, including the integrated PG degrees in the field of Life Sciences/Biomedical Sciences /Clinical Research/ Biochemistry/Public Health or related disciplines. Manipal Academy of Higher Education

Doctor of Pharmacy (Pharm D) from a recognised university Two years of experience in clinical research/ clinical trials as required for the study of the project concerned. Opportunity to join SCTIMST

Masters degree in Clinical Research / Health Sciences / Public Health / Pharmacy / Pharmaceutical Science / Biotechnology from a recognized university. SCTIMST

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