CDMA Pharmacovigilance Job At Hetero Hyderabad
Join Hetero as a CDMA – Pharmacovigilance professional in Hyderabad and play a key role in monitoring, assessing, and reporting adverse events. Ideal candidates will have 2–4 years of pharmacovigilance experience and expertise in global safety regulations, case processing, and database management. Graduates seeking M Pharma jobs or PharmD Jobs can apply for this Pharmacovigilance Job.
- Job Title: CDMA – Pharmacovigilance
- Location: Hyderabad, Telangana, India
About the Role
- Perform initial screening and validity assessment of adverse event reports from spontaneous, literature, regulatory, and clinical trial sources.
- Ensure completeness and correct seriousness classification of cases.
- Conduct duplicate checks in the Argus Safety database.
- Coordinate with cross-functional teams to resolve data gaps before processing.
- Maintain triage tracking logs and escalate priority cases.
- Enter Individual Case Safety Reports (ICSRs) accurately in the safety database.
- Perform event and product coding using MedDRA and WHO Drug dictionaries.
- Draft clear, chronological case narratives based on source documentation.
Required Skills
- Strong knowledge of global pharmacovigilance regulations and reporting timelines.
- Hands-on experience with Argus Safety database.
- Proficiency in MedDRA and WHO Drug coding.
- Analytical mindset with strong communication skills.
- Ability to manage workload within strict timelines.
Educational Requirements
-
M. Pharm or Pharm. D (with relevant pharmacovigilance experience).
Why Join Hetero?
Strengthen your pharmacovigilance career while ensuring patient safety and regulatory compliance. Collaborate with global teams and contribute to high-impact safety reporting initiatives. Graduates seeking M Pharma jobs or PharmD Jobs can apply now.
