Pfizer Hiring for Aggregate Report Coordinator in Chennai

Pfizer Healthcare India; Chennai District; On-site; INR 550,000 - 750,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

Pfizer is hiring for the role of Associate – Aggregate Report Coordinator in Chennai, a hybrid position. The role focuses on safety aggregate reporting and regulatory compliance to support global health authorities with timely submissions.

Ideal candidates have life sciences foundations and experience in drug safety, with strong project management and cross-functional collaboration skills. This assignment contributes to patient safety and regulatory excellence within a leading biopharmaceutical

Qualifications

• Experience in the pharmaceutical industry, clinical research, or healthcare environment.
• Strong knowledge of safety and regulatory reporting processes preferred.
• Excellent English verbal, written, and presentation skills.
• High attention to detail and data accuracy.
• Strong project management and issue-resolution skills.

Responsibilities

• Lead safety aggregate report preparation from initiation through final regulatory submission.
• Partner with Clinical, Regulatory, Drug Safety, Submissions, DevOps, and other functional teams.
• Review safety and clinical data to ensure consistency across multiple contributors.
• Compile report content using electronic tools and document management systems.
• Ensure reports meet regulatory standards and submission timelines.

Skills

Pharmacovigilance

Regulatory reporting

Project management

Cross-functional collaboration

Data accuracy

Education

Bachelor’s degree in Life Sciences

Tools

Microsoft Word

Microsoft Excel

Adobe Acrobat

ISI Toolbox

SharePoint

InfoPath

SharePoint Designer

Business Objects

Job description

Life Sciences Graduates Hiring – Aggregate Report Coordinator, Chennai

Life sciences graduates hiring for Associate Aggregate Report Coordinator at Pfizer. Multiple positions, Chennai hybrid role.

Pfizer is hiring Associate – Aggregate Report Coordinator professionals to strengthen its global drug safety and regulatory reporting operations. This role is ideal for life sciences and healthcare graduates who want hands‑on exposure to pharmacovigilance, safety aggregate reporting, and regulatory compliance. The position plays a critical role in ensuring timely and compliant submission of safety reports to global health authorities, directly supporting patient safety and regulatory excellence.

Company Overview

Pfizer is one of the world’s leading biopharmaceutical companies, known for developing, manufacturing, and delivering innovative medicines and vaccines that improve global health. With a strong presence across clinical research, drug safety, regulatory affairs, and medical operations, Pfizer operates at the highest standards of scientific integrity and regulatory compliance.

The organization is deeply committed to ethics, quality, and equal opportunity employment. Every role at Pfizer contributes to advancing therapies that ultimately benefit patients worldwide, making it a trusted and authoritative employer in the pharmaceutical and healthcare industry.

Job Role & Responsibilities

As an Associate – Aggregate Report Coordinator, you will be responsible for the project management and coordination of safety aggregate reports submitted to global regulators such as the FDA and EMA. This role requires strong cross-functional collaboration, attention to detail, and regulatory awareness.

Safety Aggregate Reporting

• Lead safety aggregate report preparation from initiation through final regulatory submission
• Partner with Clinical, Regulatory, Drug Safety, Submissions, DevOps, and other functional teams
• Review safety and clinical data to ensure consistency across multiple contributors
• Compile report content using electronic tools and document management systems
• Ensure reports meet regulatory standards and submission timelines

Review & Compliance Management

• Coordinate internal and external review and approval cycles for aggregate reports
• Address reviewer comments and ensure accurate incorporation of feedback
• Ensure reports are completed and submitted before regulatory due dates
• Provide guidance to contributors on report structure, requirements, and timelines
• Maintain compliance with global safety and regulatory guidelines

Project & System Support

• Participate in cross-functional projects and subject matter initiatives
• Support User Acceptance Testing (UAT) activities when required
• Complete training as per Pfizer and WSR Safety Information Management curriculum
• Maintain accurate documentation and compliance records

This role directly supports pharmacovigilance operations and ensures ongoing compliance with global drug safety regulations.

Educational Background

• Bachelor’s degree in Life Sciences, Healthcare, Pharmacy, or a related pharmaceutical discipline

Relevant courses include:
BSc Life Sciences, BSc Biotechnology, BSc Microbiology, BSc Chemistry, BPharmacy, MPharmacy, MSc Clinical Research, MSc Pharmacovigilance, MSc Regulatory Affairs, MSc Life Sciences

Experience & Skills

• Experience in the pharmaceutical industry, clinical research, or healthcare environment
• Strong knowledge of safety and regulatory reporting processes preferred
• Excellent English verbal, written, and presentation skills
• High attention to detail and data accuracy
• Strong project management and issue-resolution skills
• Ability to work effectively in cross-functional and matrix environments

Technical Skills

• Proficiency in Microsoft Word and Excel
• Working knowledge of Adobe Acrobat and ISI Toolbox
• Experience with SharePoint technologies (InfoPath, SharePoint Designer)
• Business Objects experience is an added advantage

Location & Salary

• Job Location: Chennai, Tamil Nadu
• Work Mode: Hybrid
• Employment Type: Full-time

Salary details are not disclosed by the employer. Compensation is expected to be competitive and aligned with pharmaceutical industry standards for drug safety and regulatory roles.

Frequently Asked Questions (FAQs)

Who can apply for the Aggregate Report Coordinator role?

Life sciences, pharmacy, and healthcare graduates with interest or experience in drug safety and regulatory reporting can apply.

Is this role suitable for pharmacovigilance professionals?

Yes. Candidates with pharmacovigilance, safety reporting, or regulatory experience are highly suitable.

Is this a remote role?

No. This position follows a hybrid work model based in Chennai.

Does this role involve FDA and EMA submissions?

Yes. The role supports safety aggregate reports submitted to FDA, EMA, and other global regulators.