Pharmacovigilance Jobs 2026 | Pfizer Hiring Report Coordinator Associate

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Report Coordinator Associate

🏢 Pfizer

📍 Chennai

💊 Pharmacovigilance

💼 Freshers & Experienced

Pfizer is hiring a Report Coordinator Associate for its Medical Safety & Pharmacovigilance team. This opportunity is ideal for Pharmacy and Life Sciences graduates interested in Pharmacovigilance, Drug Safety, Regulatory Reporting, Safety Aggregate Reports, and Clinical Research Operations.

📋 Job Overview

Particulars	Details
Position	Report Coordinator Associate
Company	Pfizer
Location	Chennai, India
Department	Medical Safety & Pharmacovigilance
Work Mode	Hybrid
Experience	Freshers & Experienced Candidates
Employment Type	Full-Time

💊 Key Responsibilities

Coordinate safety aggregate reports from initiation to submission.
Collaborate with Safety, Clinical, Regulatory, DevOps, and Submission teams.
Review safety data for consistency and compliance.
Support regulatory reporting activities.
Manage review cycles, approvals, and comment resolution.
Ensure timely submissions to global health authorities.
Participate in User Acceptance Testing (UAT) activities.
Support process improvement initiatives.

📑 Regulatory & Safety Reporting Activities

Aggregate Safety Report Coordination.
Pharmacovigilance Documentation Management.
Regulatory Submission Support.
Cross-functional Project Coordination.
Compliance Monitoring.
Safety Data Review.
Global Reporting Requirements.

🎓 Eligible Qualifications

B.Pharm
M.Pharm
Pharm.D
BSc Life Sciences
MSc Life Sciences
Healthcare Sciences
Pharmaceutical Sciences
Related Medical & Scientific Disciplines

💻 Technical Skills

Microsoft Word
Microsoft Excel
PowerPoint
Outlook
Microsoft Teams
SharePoint
Adobe PDF
Business Intelligence Tools (Preferred)

🌟 Why Join Pfizer?

Work with a leading global biopharmaceutical company.
Exposure to global pharmacovigilance operations.
Hybrid working model.
Career growth in Drug Safety and Regulatory Affairs.
International collaboration opportunities.
Strong learning and development programs.

📈 Career Path

Report Coordinator Associate
Drug Safety Associate
Pharmacovigilance Specialist
Safety Reporting Specialist
Senior Pharmacovigilance Associate
Safety Lead
Global Pharmacovigilance Manager

📝 Resume Tips

Highlight Pharmacovigilance, Clinical Research, or Regulatory Affairs exposure.
Mention safety reporting, documentation, or coordination experience.
Include internships, certifications, or projects related to Drug Safety.
Showcase communication and project management skills.
Mention proficiency in MS Office and documentation tools.
Keep your resume ATS-friendly and achievement-focused.

🎯 Interview Preparation Tips

Review Pharmacovigilance fundamentals and safety reporting concepts.
Understand aggregate safety reports and regulatory submissions.
Learn basics of FDA and EMA reporting requirements.
Understand UAT and validation concepts.
Prepare examples demonstrating coordination and communication skills.
Research Pfizer and its global safety operations.
Revise Clinical Research and Drug Safety workflows.

❓ Common Interview Questions

What is Pharmacovigilance?
What are Aggregate Safety Reports?
What is the purpose of regulatory reporting?
What is an adverse event?
What is UAT (User Acceptance Testing)?
How would you manage multiple reporting deadlines?
Why do you want to join Pfizer?
How do you ensure accuracy in documentation?
What do you know about FDA and EMA?
Where do you see your career in Drug Safety?

❓ Frequently Asked Questions (FAQ)

Q1. Are freshers eligible?
Yes, freshers and experienced candidates can apply.

Q2. Which location is hiring?
Chennai, India.

Q3. Which qualifications are eligible?
B.Pharm, M.Pharm, Pharm.D, BSc/MSc Life Sciences, Healthcare Sciences, and related disciplines.

Q4. Is Pharmacovigilance experience mandatory?
No, relevant healthcare, clinical research, or drug safety exposure is preferred but not mandatory.

Q5. What skills are preferred?
Safety reporting, regulatory documentation, communication, project coordination, and MS Office proficiency.

📝 How to Apply

Carefully review the job description.
Update your resume with Pharmacovigilance, Clinical Research, and Regulatory experience.
Highlight safety reporting, documentation, and coordination skills.
Mention internships, certifications, and relevant projects.
Apply only if your qualifications align with the role requirements.

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