Design and evaluate oncology clinical trial frameworks — including study protocols, patient enrollment strategies, and regulatory compliance considerations
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
PGs, PharmD, MPharm Pharmacology/Pharmacy Practice with some experience in clinical research and other Life Sciences PG degrees with clinical research experience. Division of Clinical Pharmacology, Department of Pharmacology, Kasturba Medical College (KMC), Manipal.
Masters degree in Pharmacology/ Clinical Pharmacology/ Pharmacy Practice/Clinical Research. OR Pharm.D/ MBBS/ BDS from a recognized University/Institute. 1 year experience in drug safety/ Pharmacovigilance. Indian Pharmacopoeia Commission
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