The responsibilities include, but are not limited to, providing overall planning and strategic oversight of clinical study, including the development of detailed study plans, budget management, and coordination of Clinical Trial Coordinators across multiple sites.
Post Graduate degree in Science (M.Pharm, Life Sciences, Biotech, Zoology, Botany etc.) with PG Diploma in Clinical Research is mandatory with minimum 2 years experience in Clinical Trials.
BSc / B. Pharm (PG Diploma in Clinical Research is mandatory) / MSc / MPharm (PG Diploma in Clinical Research is Mandatory) / M.Sc. in Clinical Research or Equivalent Qualification
Masters degree in Pharmacy or Clinical research. Plan and perform vendor qualification and audits for pre-clinical, clinical, and In-vitro studies service providers.
Jawaharlal Institute of Postgraduate Medical Education and Research, JIPMER. Excellence in Competency-Based Medical Education EXCEL-CBME Hybrid II Implementation Study. Post graduation in Clinical Research
Graduation in Science (B.Pharm, Life Sciences. Biotech, Zoology, and Botany) with PG diploma in Clinical Research with interest in monitoring of interventional clinical trials (RCTs).
PG in Science M.Pharm, M.Sc. in Life Science, Clinical Research Regulatory Affairs with 65% plus Diploma in Clinical Research and Pharmacovigilance Activity from recognized university. 1 years’ experience in Clinical research or IEC management is mandatory.