BHMS

MBBS or Any Medical Graduate (BAMS/BUMS/BHMS/BDS/BPTH/Nursing Basic/(P.B.B.Sc)/B.Pharm + with MPE/MME/MBA in Health Care Administration)

Masters degree/ diploma, life sciences, pharmacy, public health, healthcare for clinical trial monitoring or clinical trial / study coordinator, or clinical trial/study associate. THSTI

Life Sciences with a minimum of two years of experience in clinical research, OR Professional degree in MBBS, BDS, BVSc, BAMS, BHMS, BUMS, BSMS, BNYS, B.Sc. Nursing, BPT, B.Pharm, with a minimum of one year of experience in clinical research

B.Pharm / M.Pharm graduate with experience in case processing in ARGUS, experience in global submission to Health authorities.

Postgraduate degree in Science/ Pharmacology/ Life Sciences/ Regulatory Science/ Public Health from a recognised University with atleast 6 years of relevant work experience

Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data. Be fully competent to perform all steps within the case-handling processing.

TCS opening for Pharmacovigilance Drug Safety. M.Pharm, B.Pharm, MSc. accessing the case in Argus, code and enter data.

BDS / BHMS / BAMS / B.Pharma / MBA with at least 3-years experience of handling research projects especially clinical or vaccine trials 

Masters Degree or PG Diploma or PhD in Life Sciences / Biomedical Sciences / Pharmacy / Public Health / Clinical Research with at least five years of experience in clinical project management and/or clinical trial/ study monitoring.