Bausch + Lomb
5 Years+
Bausch + Lomb
5 Years+
Maiora Clinical Research
2–4 Years
Clinovo
2–4 years
Sarthak Biotech
0 - 2 Years+
IQVIA
3 - 7 Years+
Wipro
1–2 years
Opella
1 - 7 Years
Novartis
2–5 years’ experience in Clinical Research, Pharmacovigilance, Regulatory Affairs, or Pharma Compliance, clinical trials, GCP, regulatory interactions, and drug development
Syneos Health
2 to 4 years
7 - 12 LPA
Wipro
2–4 Years
Pharmacovigilance jobs focus on detecting, assessing and communicating medicine-safety information. PharmaBharat lists opportunities for freshers and experienced professionals in drug safety, case processing, medical review, safety writing and related operations across India.
Related career areas: Clinical Research · Medical Writing · Regulatory Affairs
Common roles include Drug Safety Associate, Patient Safety Associate, PV Operations Associate, Safety Data Specialist and Medical Reviewer. Employers may consider B.Pharm, M.Pharm, Pharm.D, medicine, nursing, biotechnology and other life-sciences graduates, depending on the role.
Yes. Entry-level roles include trainee, case-processing and drug-safety associate positions. Employers usually look for medical terminology, documentation accuracy and an understanding of adverse-event reporting.
B.Pharm, M.Pharm, Pharm.D and related life-sciences qualifications are commonly relevant. The exact eligibility, shift pattern and experience requirement should be checked in each vacancy.