Bachelor degree in clinical research Or Social sciences or Biotechnology. Experience in working projects / programs. Demonstrated ability to liaison with different and multiple organizations
First class Post Graduate Degree, Including the integrated PG degree in Optometry, Biotechnology, Microbiology, Medical biochemistry, Clinical Pharmacology or Clinical Research.
MSc in Life Science / M.Pharm. PG Diploma in Clinical research is Mandatory Or Msc in Clinical research. Required IEC Co-ordinator, under, Institutional Ethics Committee
Masters degree / PG Diploma in Life Sciences / Pharmacy / Public Health / Healthcare or related discipline with minimum two years of relevant clinical trial monitoring experience.
Post Graduate degree with PG diploma in Clinical Research / M.Sc in Clinical Research or equivalent qualification. 3 years' experience in clinical research in clinical research is mandatory. Willing to work on outreach project.
MSc / MPharm (PG Diploma in Clinical Research is mandatory) / MSc in Clinical Research/ MBBS/ BDS/ BAMS/ BHMS/ BUMS (PG Diploma in Clinical Research is Mandatory) or PharmD or Equivalent Qualification
MSc Clinical Research, and age less than 30 years. Candidates with experience of working as Clinical Research Coordinator in a Clinical Trial will be given preference
Preferably PharmD with Experience in Coordinating and conducting clinical trials. Conducting and coordinating clinical trials in the department of Medical Oncology.
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.