Looking for an exciting Senior Specialist Pharmacovigilance opportunity in Hyderabad? ProPharma is hiring experienced Pharmacovigilance professionals for its Case Processing team. This is an excellent opportunity for candidates with experience in ICSR processing, Argus Safety, MedDRA coding, medical narrative writing, and regulatory reporting to work with a leading global life sciences consulting organization.
If you have expertise in drug safety, adverse event case processing, quality review, and global pharmacovigilance regulations, this opportunity could help you advance your pharmacovigilance career.
Job Details
| Particular | Details |
|---|---|
| Position | Senior Specialist โ Pharmacovigilance |
| Company | ProPharma Group |
| Job Location | HITEC City, Hyderabad |
| Employment Type | Full Time |
| Experience | 2โ6 Years |
| Qualification | B.Pharm or Bachelor’s Degree in Life Sciences |
| Preferred Qualification | PharmD, RPh, RN, Advanced Life Sciences Degree |
| Openings | 5 |
| Industry | Pharmaceutical & Life Sciences |
Key Responsibilities
The selected candidates will be responsible for:
- Perform end-to-end Individual Case Safety Report (ICSR) processing.
- Conduct peer review and quality checks of adverse event cases.
- Perform MedDRA coding for adverse events.
- Determine seriousness, causality, and expectedness of safety cases.
- Prepare accurate and comprehensive medical narratives.
- Generate case queries for missing safety information.
- Ensure expedited regulatory submissions as per global PV regulations.
- Perform follow-up activities for incomplete cases.
- Support client notifications and case management activities.
- Mentor and train junior pharmacovigilance professionals.
- Review Health Care Professional (HCP) cases whenever required.
- Ensure compliance with SOPs, GVP guidelines, and regulatory requirements.
- Collaborate with cross-functional pharmacovigilance teams.
Required Qualifications
Candidates should possess:
- Bachelor’s Degree in Life Sciences or B.Pharm.
- Minimum 3 years of Pharmacovigilance experience.
- Experience in ICSR case processing.
- Knowledge of MedDRA coding.
- Experience with Oracle Argus Safety, ARISg, or similar safety databases.
- Strong understanding of global Pharmacovigilance regulations.
- Good communication and analytical skills.
- Ability to mentor junior team members.
Preferred Qualifications
- PharmD
- Registered Pharmacist (RPh)
- Registered Nurse (RN)
- Master’s Degree in Life Sciences
Required Skills
- Pharmacovigilance
- Drug Safety
- ICSR Processing
- Case Processing
- Medical Narrative Writing
- MedDRA Coding
- Oracle Argus Safety
- ARISg
- Regulatory Reporting
- Seriousness Assessment
- Expectedness Assessment
- Literature Review
- Quality Review
- Global PV Regulations
- SOP Compliance
Why Join ProPharma?
Working with ProPharma offers several career advantages:
- Opportunity to work on global pharmacovigilance projects.
- Exposure to international safety reporting standards.
- Career growth in drug safety operations.
- Collaborative work environment.
- Learning opportunities with experienced PV professionals.
- Experience with leading safety databases and regulatory requirements.
Salary
Based on similar Pharmacovigilance Senior Specialist roles in Hyderabad, the expected salary ranges between:
โน6,00,000 โ โน10,00,000 per annum (CTC)
Actual compensation depends on experience, technical expertise, and interview performance.
How to Apply
