CR

Towards accurate determination of burden of kidney disease in India, Development and validation of accurate equation to estimate glomerular filtration rate, GFR, for Indian population. A three year bachelors degree in Paramedical sciences/ Life Sciences / B.Pharm/ B.Sc Nursing

Homi Bhabha Cancer Hospital & Research Centre, Aganampudi, Visakhapatnam recruitment; Graduate in Science E.g. B.Pharm, Life science, B.Sc., Biotech, Zoology, Botany, etc., with PG Diploma in Clinical Research is preferable.

Masters degree in Pharmacy/ Clinical Pharmacology/ Pharmacy Practice/ Clinical Research OR Pharm.D; experience in Pharmacovigilance with Good communications and knowledge of computers.

BHMS, BAMS, BUMS, BDS, B.Sc Life science, M.Sc, Life Science, B.Pharma., D.Pharma and Diploma in Clinical Research.

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.