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If you’re looking to advance your career in pharmacovigilance case processing, this opportunity at ProPharma Group in Hyderabad could be a strong fit. With increasing global focus on drug safety and regulatory compliance, skilled PV professionals are in high demand. This role offers hands-on exposure to ICSR processing, MedDRA coding, and safety reporting, making it ideal for candidates with 2+ years of pharmacovigilance experience.
๐ Job Overview
- Role: Pharmacovigilance Specialist
- Company: ProPharma Group
- Location: Hyderabad (Madhapur), India
- Experience: 1โ4 years
- Employment Type: Full-time, Permanent
- Openings: 5
๐ Key Responsibilities (Pharmacovigilance Case Processing)
As a Pharmacovigilance Specialist, you will:
- Perform adverse event case processing (clinical trial & post-marketing)
- Conduct case-level assessment (seriousness, expectedness)
- Create detailed medical narratives
- Code adverse events using MedDRA
- Handle ICSR processing and regulatory submissions
- Generate follow-ups for missing safety data
- Ensure compliance with global pharmacovigilance regulations
- Perform peer review of safety cases
- Collaborate with cross-functional teams for quality case management
๐ Qualifications & Skills
Educational Requirements:
- Bachelorโs degree in Life Sciences / B.Pharm
- Preferred: PharmD, M.Pharm, or equivalent
Experience:
- Minimum 2 years in pharmacovigilance case processing
- Experience with ICSR, MedDRA coding, safety databases
Key Skills:
- Strong understanding of drug safety & pharmacovigilance workflows
- High attention to detail and accuracy
- Excellent written & verbal communication
- Ability to manage multiple cases efficiently
๐ผ Salary & Benefits
- Estimated Salary: โน3,50,000 โ โน6,50,000 per annum (based on industry standards for PV roles)
- Exposure to global pharmacovigilance projects
- Career growth in drug safety and regulatory affairs
- Opportunity to work with international clients
- Training and upskilling in ICSR compliance and safety systems
๐ Why This Role Matters
With increasing regulatory scrutiny worldwide, pharmacovigilance specialists play a critical role in ensuring patient safety. This job enhances your expertise in:
- ICSR lifecycle management
- Global safety reporting standards
- Regulatory compliance (FDA, EMA, ICH guidelines)
๐ฉ How to Apply
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