Advanced knowledge of Data Management processes and systems. Solid understanding of clinical drug development process and production of Data Management deliverables
B.Pharma + M.Pharma , M.Sc. / Master’s degree in Pure or Applied Sciences, including Biochemistry, Biotechnology, Microbiology, Nursing, and other relevant Life Sciences disciplines, MBBS degree or a Doctorate in Pure or Applied Sciences.
Office-based Clinical Safety Coordinator to join our Clinical Safety department in India. This position will be focused on the handling and processing of adverse events from all sources, including clinical trials and post marketing surveillance.
Graduate Degree in Life Sciences / Pharmacology /Public Health/ Nursing including the integrated PG degrees. Dept of Pediatrics, AIIMS Bhubaneswar. ESCHAR Trial
The Manager, Regulatory Affairs provides project representation and input to projects awarded to WCT for all stages of the drug development cycle and ensures the smooth running of the Regulatory Affairs Department