CR

Bachelor or Master Degree -MS/MA- Science Field. Support protocol amendments, Investigators Brochure updates, and Informed Consent Form revisions. Maintain Trial Master File, TMF and ensure timely filing and quality control of essential documents

Postgraduate degree in Science (M. pharm, Life Sciences, Biotech, Zoology, Botany, etc.) with PG Diploma in Clinical Research is mandatory. Homi Bhabha Cancer Hospital & Research Centre

BSc, MSc, B.Pharma, M.Pharma or degree/ diploma in Clinical Research. At least 1 year of experience at clinical trial sites. PGIMER

First Class Post Graduate Degree, including the integrated PG degree/ with PhD in Clinical research/ pharmacology and three yrs experience in clinical trials and clinical data management. AIIMS, Delhi

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

Bachelors or masters degree in Life Sciences (e.g., Biomedical Engineering, Nursing, Medicine, Pharmacy). Zydus Lifesciences

Bachelors or Masters degree in life sciences, natural sciences, engineering, or equivalent qualifications. 2-3 years of programming experience, preferably working with biological data or equivalent knowledge through relevant practical experience. 

Bachelors Degree Clinical, biological. Provide basic and some comprehensive data management expertise to the Clinical Data Management, CDM team to provide efficient, quality data management products that meet customer needs. IQVIA

B. Pharm (PG Diploma in Clinical Research is mandatory) / M.Sc. / M. Pharm (PG Diploma in Clinical Research is Mandatory)/ M.Sc. in Clinical Research or Equivalent Qualification Monthly