Aggregate Report Analyst Manager – Join Pfizer’s Global Safety and Regulatory Team in Chennai-Apply Now

About Pfizer

Pfizer is a global biopharmaceutical leader driven by science, innovation, and a mission to deliver breakthroughs that change patients’ lives. With operations across 120+ countries, Pfizer is at the forefront of discovering, developing, and delivering safe, effective medicines and vaccines that advance global health.

Now, Pfizer is inviting applications for the position of Aggregate Report Analyst Manager in Chennai, India — a pivotal role in the Worldwide Safety (WWS) division. This opportunity is perfect for professionals passionate about pharmacovigilance, safety data analysis, and global regulatory documentation.

💊 Position Overview

As an Aggregate Report Analyst Manager, you will play a key role in the preparation and submission of global safety documents, ensuring compliance with international pharmacovigilance and regulatory standards.
This role is ideal for individuals experienced in post-marketing safety, clinical trials, or regulatory writing who want to take their expertise to the next level with one of the world’s most respected pharmaceutical organizations.

Key Responsibilities

• Prepare and deliver aggregate safety documents, including DSURs, PBRERs, PSURs, RMPs, ACOs, and regulatory safety responses.

• Ensure full compliance with internal SOPs, Pfizer quality standards, and global regulatory requirements.

• Collaborate with cross-functional teams, including safety physicians, epidemiologists, and regulatory writers, to maintain accuracy and consistency in submissions.

• Provide oversight and guidance to co-authors and vendors during report preparation and review.

• Translate complex safety data into clear, factual, and concise regulatory documents.

• Serve as the point of contact for assigned products, managing timelines, strategy, and document quality.

• Support process optimization and quality improvement initiatives within Worldwide Safety (WWS).

🎓 Required Qualifications

Education:

• Bachelor’s degree in Life Sciences with at least 3 years of relevant medical/pharmaceutical experience.

• Advanced degree (MD, PharmD, PhD, or MSc) preferred.

Experience & Skills:

• Strong understanding of pharmacovigilance principles and global regulatory reporting requirements.

• Proven experience in clinical trial safety, post-marketing surveillance, or regulatory writing.

• Analytical ability to interpret safety data and synthesize complex findings into structured reports.

• Excellent scientific writing, editing, and communication skills.

• Strong organizational skills with the ability to manage multiple projects and deadlines simultaneously.

• Proficiency in working with global cross-functional teams in a regulated environment.

🌍 Why Join Pfizer?

• Work with a world-class team advancing global drug safety and regulatory excellence.

• Contribute to life-saving medicines and innovations that impact millions of patients.

• Experience a collaborative, inclusive, and purpose-driven culture.

• Access to continuous learning, training, and professional development opportunities.

• Enjoy a competitive compensation package, performance-based rewards, and comprehensive employee benefits.

💼 Job Details

• Position: Aggregate Report Analyst Manager

• Location: Chennai, Tamil Nadu, India

• Division: Worldwide Safety (WWS)

• Experience Required: 3+ years

• Employment Type: Full-time

• Date Posted: October 4, 2025

📝 How to Apply

If you’re ready to advance your career in pharmacovigilance and regulatory writing with Pfizer, apply through the official career portal:
🔗 Apply Here

🌟 Be Part of Something Extraordinary

At Pfizer, your work shapes the future of global healthcare. Join a team that combines scientific excellence, integrity, and innovation to make a meaningful impact on lives worldwide.

Pfizer – Breakthroughs That Change Patients’ Lives.