Clinical Research

Review clinical trial protocols, visit schedules, enrollment assumptions, country requirements, and other study documentation to determine whether and how Labcorp Smart Supply should be used.

Degree with life Science background, trained in Clinical research e.g. Diploma in clinical research , or MSC Clinical research and PharmD

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