If you’re aiming to build a career in Medical Information, Pharmacovigilance (PV), and Medical Affairs, this opportunity at Pharmazone offers strong exposure to global pharma processes, safety reporting, and regulatory compliance.
Pharmazone, a globally recognized consulting firm in Regulatory Affairs, Pharmacovigilance, and GxP Compliance, is hiring a Medical Information Specialist for its Ahmedabad office. This role is ideal for candidates looking to work on ARIS-g, TrackWise, IRMS systems, adverse event handling, and medical inquiry management.
🔑 Key Responsibilities (Medical Information & PV Role)
- Manage and process medical inquiries received via phone, email, fax, or mail
- Create and maintain records in IRMS (Inquiry Response Management System) and TrackWise
- Handle adverse event (AE) intake and case booking in ARIS-g safety database
- Perform triage of safety cases and ensure proper documentation (AEM forms)
- Follow Good Documentation Practices (GDP) and TrackWise conventions
- Attach supporting documents like product replacement forms and source documentation
- Maintain voicemail tracking and reporting dashboards
- Generate periodic reports on inquiries and complaint trends
- Use FAQs, product labels, and scientific data to respond to medical queries
- Ensure compliance with global pharmacovigilance and regulatory requirements
🎓 Qualifications & Skills Required
- Educational Qualification: B.Pharm / M.Pharm / Life Sciences / Medicine
- Strong knowledge of:
- Pharmacovigilance (ICSR processing basics)
- Medical Information & Medical Affairs
- Regulatory compliance & safety reporting
- Hands-on or theoretical understanding of:
- ARIS-g, TrackWise, IRMS systems
- Excellent communication and scientific writing skills
- Ability to work in night shifts (global support environment)
- Experience in medical communications or drug safety is preferred
💼 Salary & Benefits (Estimated)
- 💰 Salary Range: ₹3.5 LPA – ₹6.5 LPA (based on experience)
- 🌍 Exposure to global clients (US, EU, Canada markets)
- 📈 Career growth in Pharmacovigilance, Medical Information, Regulatory Affairs
- 🧠 Training on industry tools (ARIS-g, TrackWise)
- 🤝 Opportunity to work in a consulting-driven pharma environment
🚀 Why This Role is High-Value for Pharma Careers
This Medical Information Specialist job in Ahmedabad is strategically important for candidates targeting:
- Pharmacovigilance (PV Associate / Drug Safety roles)
- Medical Writing & Medical Communications
- Regulatory Affairs & Safety Reporting
- Clinical Research & Post-Marketing Surveillance
You gain end-to-end exposure from inquiry intake → AE reporting → database entry → compliance, which is critical for CRO and pharma company roles.
📩 How to Apply
Interested candidates can apply by sending theirupdated CVto the official email address:
