CR

DPharm/B Pharma/Pharm D graduate Five years experience in relevant subject/field

An initiation Clinical Research Associate (iCRA) specializing in Pre SIV and Activation tasks will be assigned & accountable for managing and driving the strategy for the startup, Pre SIV and Activation tasks of the study. The iCRA also supports submission and approval process for the protocol amendments if applicable.

Preferably PharmD with Experience in Coordinating and conducting clinical trials. Conducting and coordinating clinical trials in the department of Medical Oncology.

MPharma / MSc in life science or equivalent. OR Graduate in life science (BAMS/BHMS/BSc Nursing/ BPT or equivalent) from a recognized university with three years of experience from a recognized institute.

M.Sc. in Clinical Research, M.Pharm / M.Tech / M.Sc. in Life Sciences with focus on Clinical Research/ MPH or Health & Hospital Management

MSc in Biotechnology, Microbiology, Biochemistry. Minimum 6 months to 1 year experience in clinical research / clinical trials.

Bachelors in Life Sciences with relevant clinical trial monitoring or clinical trial/study coordinator, or clinical trial/study associate experience. Masters degree/ diploma, life sciences, pharmacy, public health, healthcare

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

clinical data cleaning and reconciliation activities performed with high accuracy and in accordance with GCP, SOPs/WPDs, and study protocols. experience in RAVE / Veeva EDC