Indian Council of Medical Research (ICMR) is an Autonomous Organization, under the Department of Health Research, Ministry of Health & Family Welfare, Govt. of India. ICMR is dealing with biomedical/ health research in various areas, in collaboration with National/ International agencies, through its Headquarters at New Delhi and 28 Institutes/Centres and a large number of field stations, situated across the country.
Build electronic health record query to support protocol design and feasibility process. Provide insights as to data quality/availability and feasibility of specific use cases to stakeholders and assess the reliability of methods used
Develop and review Data Management procedures for clinical trials with sponsor companies and other departments; Establish/negotiate Data Management project timelines and ensure Data Management milestones are met
Bachelors or Masters degree in Life Sciences, Pharmacy, Medicine, Nursing, or a related discipline. 2–5 years of experience in pharmacovigilance, case management, or related regulated operations.
Ph.D. or Master in Life Sciences, Biotechnology, Pharmacology, or related field. Strong understanding of the drug discovery pipeline and integrated biology workflows.
Masters in pharma / Biotechnology / Chemistry at Dr. Reddys Lab. Seeking a dynamic and experienced Specialist in Process Development in the pharmaceutical development process, responsible for strategy evaluations, process design, optimization