Pfizer Hiring Aggregate Report Analyst Senior Associate – Life Sciences

Aggregate Report Analyst Senior Associate – Life Sciences | Pfizer | 2+ Years Experience | Chennai, India

Apply for Aggregate Report Analyst – Senior Associate role at Pfizer in Chennai. Open to Life Sciences graduates with 2+ years’ experience in medical writing, safety, or regulatory.

Aggregate Report Analyst Senior Associate – Join Pfizer’s Safety and Regulatory Team

Pfizer, one of the world’s premier innovative biopharmaceutical companies, is hiring a Senior Associate – Aggregate Report Analyst for its Chennai location. This full-time role is an opportunity for experienced professionals in life sciences to contribute to global post-marketing safety initiatives within a highly regulated and collaborative environment.

The role focuses on the creation and oversight of regulatory safety documents supporting product development, license applications, and ongoing safety assessments. Ideal candidates will have 2+ years of experience in clinical research, pharmacovigilance, regulatory affairs, or medical writing, preferably with exposure to safety reporting.

📍 Job Location

Location: Chennai, India
Position Type: Full-Time, Senior Associate

Job Role Overview

As part of Pfizer’s Worldwide Safety (WWS) division, the Aggregate Report Analyst will contribute to the preparation and review of regulatory safety documents such as:

• Development Safety Update Reports (DSURs)
• Periodic Safety Update Reports (PSURs)
• Periodic Benefit-Risk Evaluation Reports (PBRERs)
• Addendum to Clinical Overviews (ACO)
• Risk Management Plans (RMPs)
• Canadian Annual Reports

This role involves collaboration with cross-functional project teams to ensure compliant and timely document delivery.

Key Responsibilities

• Create high-quality, regulatory-compliant documents involving safety data
• Interpret safety analyses and synthesize clear, concise content
• Identify information gaps and strategize solutions with internal teams
• Ensure delivery of documents within agreed timelines and standards
• Provide oversight for vendor-produced content and offer performance feedback
• Drive key messaging collaboratively with subject matter experts
• Collaborate with global quality and regulatory teams to ensure alignment

Required Qualifications

• Bachelor’s Degree in Life Sciences (e.g., Pharmacy, Biology, Biochemistry, Biotechnology)
• Advanced degree preferred (MD, DVM, PharmD, or Master’s/PhD in a relevant field)

Experience Requirements

• Minimum of 2 years’ experience in:
  • Medical writing
  • Pharmacovigilance or safety analysis
  • Clinical trials or regulatory documentation
• Understanding of global regulatory requirements and pharmacovigilance practices
• Familiarity with benefit-risk assessment strategies
• Strong writing and analytical skills for interpreting clinical data

Ideal Candidate Profile

• Strong ability to translate scientific data into regulatory language
• Familiar with tools and templates used in medical writing and safety submissions
• Works well under general supervision, with growing independence
• Able to handle multiple projects and prioritize deadlines

Why Join Pfizer?

• Work with one of the top global leaders in pharmaceuticals
• Be part of a culture driven by science, innovation, and ethical standards
• Opportunity to collaborate with global safety and regulatory teams
• Build your career in a company known for development opportunities and employee wellbeing

Apply here 

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