Pharmacovigilance Jobs 2026 | Glenmark Hiring Officer – Pharmacovigilance

Mohit June 10, 2026
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Pharmacovigilance Jobs 2026 | Glenmark Hiring Officer – Pharmacovigilance
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Officer – Pharmacovigilance

🏢 Glenmark
📍 Navi Mumbai
💊 Pharmacovigilance
💼 2–3 Years

Glenmark Pharmaceuticals is hiring an Officer – Pharmacovigilance for its R&D division in Navi Mumbai. This opportunity is ideal for professionals with experience in ICSR Processing, Clinical Trial Safety, SAE Reconciliation, Safety Reporting, and Global Pharmacovigilance Operations.

📋 Job Overview

Particulars Details
Position Officer – Pharmacovigilance
Company Glenmark Pharmaceuticals
Location Mahape, Navi Mumbai
Experience 2–3 Years
Qualification M.Pharm, B.Pharm, Master's Degree in Health Sciences
Employment Type Full-Time
Salary ₹5.0 – ₹6.5 LPA (Estimated)

💊 Pharmacovigilance Responsibilities

  • Support global pharmacovigilance activities.
  • Process and manage Individual Case Safety Reports (ICSRs).
  • Handle adverse event reporting and follow-up activities.
  • Support clinical safety regulatory submissions.
  • Participate in safety review meetings.
  • Assist with Safety Management Plans (SMPs).

🔬 Clinical Trial Safety Activities

  • Support clinical project teams on safety activities.
  • Conduct SAE follow-up and tracking.
  • Participate in SAE reconciliation activities.
  • Coordinate with Data Management teams.
  • Resolve reconciliation discrepancies.
  • Support database lock reconciliation processes.

📑 Documentation & Compliance

  • Maintain TMF/eTMF documentation.
  • Support ISMF management activities.
  • Maintain safety records and archives.
  • Manage pharmacovigilance mailboxes.
  • Support SOP development and compliance initiatives.
  • Assist during audits and inspections.

🎓 Eligible Qualifications

  • M.Pharm
  • B.Pharm
  • Master's Degree in Health Sciences

⭐ Required Skills

  • ICSR Processing
  • SAE Reconciliation
  • Clinical Trial Safety
  • Pharmacovigilance Regulations
  • TMF/eTMF Management
  • Microsoft Office
  • Documentation Review
  • Communication Skills

🌟 Why Join Glenmark?

  • Exposure to global pharmacovigilance operations.
  • Work closely with clinical and regulatory teams.
  • Career growth in drug safety and clinical safety.
  • Experience in clinical trial safety management.
  • Learning opportunities within R&D functions.
  • Professional development and industry exposure.

📈 Career Path

  • Drug Safety Associate
  • Pharmacovigilance Officer
  • Senior Pharmacovigilance Officer
  • Drug Safety Specialist
  • Safety Scientist
  • Pharmacovigilance Manager
  • Global Safety Lead

📝 Resume Tips

  • Highlight ICSR processing and case management experience.
  • Mention SAE reconciliation and clinical trial safety activities.
  • Include pharmacovigilance software and safety database experience.
  • Showcase TMF/eTMF and regulatory documentation exposure.
  • Mention ICH-GCP, FDA, and global PV regulations knowledge.
  • Keep your resume ATS-friendly and achievement-focused.

🎯 Interview Preparation Tips

  • Revise ICSR processing workflow and timelines.
  • Understand SAE reconciliation procedures.
  • Review clinical trial safety reporting requirements.
  • Learn ICH-GCP and pharmacovigilance regulations.
  • Understand TMF/eTMF documentation processes.
  • Review signal detection and case follow-up concepts.
  • Research Glenmark's therapeutic areas and R&D activities.

❓ Common Interview Questions

  1. What is Pharmacovigilance?
  2. What is an ICSR?
  3. What is SAE reconciliation?
  4. What are expedited reporting timelines?
  5. What is the difference between AE and SAE?
  6. What is a Safety Management Plan (SMP)?
  7. What is the purpose of TMF/eTMF?
  8. How do you ensure data quality in safety reporting?
  9. Why do you want to join Glenmark?
  10. How do you manage multiple safety cases simultaneously?

❓ Frequently Asked Questions (FAQ)

Q1. What experience is required?
Candidates should have 2–3 years of Pharmacovigilance experience.

Q2. Which location is hiring?
Mahape, Navi Mumbai, Maharashtra.

Q3. Which qualifications are eligible?
M.Pharm, B.Pharm, and Master's Degree in Health Sciences.

Q4. What are the key skills required?
ICSR Processing, SAE Reconciliation, Clinical Trial Safety, TMF/eTMF Management, and Regulatory Compliance.

Q5. What is the estimated salary range?
Approximately ₹5.0–₹6.5 LPA based on experience and company policies.

📝 How to Apply

  • Review the complete job description carefully.
  • Update your resume with Pharmacovigilance and Clinical Safety experience.
  • Highlight ICSR processing, SAE reconciliation, and safety reporting activities.
  • Mention regulatory compliance and documentation experience.
  • Apply before the position closes.

👉 Step-by-Step Guide: How to Apply for Healthcare & Pharma Jobs

🚀 Apply Now

📝 Apply for Officer – Pharmacovigilance
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