CR

Pharm.D With 1 year experience in Clinical Research. An Open-Label, Single-Arm, Prospective, Multicenter, Phase III Study to Evaluate the Efficacy, Safety and Pharmacokinetics of Human Normal Immunoglobulin for Intravenous Use in Adult and Paediatric Subjects with Primary Immunodeficiency Syndrome

Masters degree / PG Diploma in Life Sciences / Pharmacy / Public Health / Healthcare or related discipline with minimum two years of relevant clinical trial monitoring experience.

Pharm-D, M.Pharm, M.Tech (Life sciences) (Minimum of 6 months to 1 year experience) 

B.Sc / B.Pharm (PG Diploma In Clinical Research is Mandatory) or equivalent qualification.

BSc, M.Sc, M.Pharm, B.Pharm., or degree/diploma in clinical research. Atleast 1 year of experience at clinical trial sites.

Masters degree in Science. 3 years of experience in clinical research, data entry, or relevant technical support roles

Master degree in Pharmacology / Clinical Pharmacology / Pharmacy Practice / Clinical Research. OR Pharm.D/ MBBS/BDS from a recognized university / institute.

Masters Degree in Public Health / Life Sciences / Clinical Research / Social Sciences / Epidemiology. PhD in a relevant stream mentioned above.

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