CR

Graduation in science; B.Pharm., Life science, B.Sc., Bio-Tech, zoology, botany etc., with PG diploma in clinical research is desirable.; Working in collaboration with the PI and with a multidisciplinary research team to ensure that rigorous clinical research standards are maintained. Pre-screening and helping in enrolling subjects, participants in studies and managing their participation according to ethical, regulatory, Institution SOP and protocol-specific requirements.

Ensure that the correct suspect drug was selected within the Pharmacovigilance Safety System; Code medical terms using standardized medical dictionaries i.e. MedDRA Using medical expertise, ensure that all data has been entered and coded correctly in the Global Safety Database

M.Pharm or MBBS; Multicentre Performance evaluation of Diagnostic Accuracy of a point-of-care Urine Lipoarabinomannon Screening Assay for HIV associated Tuberculosis in India

M.Pharma/ B. Pharma / M.Sc Clinical research; Strong understanding of clinical research processes, documentation, randomization, data collection & entry from multicenter trials

As a Scientist, Clinical Trial Safety, you will play a pivotal role in reviewing large amounts of clinical data to ensure patient data is complete and medically accurate. support the team during study start-up activities, review patient-level clinical/safety data on an ongoing basis, schedule and facilitate different types of meetings, and create visualizations from applicable tools.

Physicians, Pharm.D, M.Pharm, Nursing or related Health Science discipline. Excellent analytical and problem-solving skills.

etermine biocompatibility testing required to demonstrate product safety. Document risk assessments in Baxter qualified systems such as Team Center Unified, Trackwise 8, Electronic Laboratory Notebook. Generate protocols and reports for biocompatibility testing.

M.Pharm / M.Sc; Candidates with exposure in the pharmaceutical industry with biologics, preferably in regulatory affairs for highly regulated markets.