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Senior Associate – Aggregate Report Analyst

Pfizer
2+ years
INR 8 LPA – 16 LPA
Chennai, India
1 July 2, 2026
Job Description
Job Type: Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

Senior Associate – Aggregate Report Analyst

Company: Pfizer
Location: Chennai, India (Hybrid)
Department: Worldwide Safety
Job Type: Full-Time
Experience: 2+ Years


JOB OVERVIEW

The Senior Associate – Aggregate Report Analyst is responsible for preparing high-quality aggregate safety reports, benefit-risk assessments, and regulatory safety documents to support product development, marketing authorization, and post-marketing pharmacovigilance activities. The role involves analyzing clinical and post-marketing safety data, collaborating with cross-functional global teams, ensuring compliance with international regulatory guidelines, and contributing to the preparation of documents such as DSURs, PBRERs, PSURs, Risk Management Plans (RMPs), and regulatory responses.


KEY RESPONSIBILITIES

Aggregate Safety Reporting

  • Prepare Development Safety Update Reports (DSURs).

  • Prepare Periodic Benefit-Risk Evaluation Reports (PBRERs).

  • Prepare Periodic Safety Update Reports (PSURs).

  • Develop Risk Management Plans (RMPs).

  • Prepare Addenda to Clinical Overviews (ACOs).

  • Support NDA Periodic Adverse Drug Experience Reports (PADERs).

  • Generate post-marketing safety assessment documents.

Safety Data Analysis

  • Analyze clinical trial safety data.

  • Evaluate post-marketing safety information.

  • Perform integrated safety analyses.

  • Interpret benefit-risk profiles.

  • Identify emerging safety trends.

  • Support signal evaluation activities.

  • Summarize complex safety datasets.

Benefit-Risk Assessment

  • Conduct benefit-risk evaluations.

  • Prepare scientific safety summaries.

  • Support regulatory decision-making.

  • Present evidence-based safety conclusions.

  • Ensure consistent benefit-risk messaging.

Regulatory Documentation

  • Prepare regulatory safety submissions.

  • Draft responses to regulatory authority queries.

  • Ensure compliance with ICH, FDA, and EMA guidelines.

  • Maintain regulatory documentation quality.

  • Support global regulatory submissions.

Cross-Functional Collaboration

  • Partner with Pharmacovigilance teams.

  • Collaborate with Regulatory Affairs.

  • Coordinate with Medical Affairs.

  • Work with Clinical Development teams.

  • Liaise with Epidemiology and QPPV teams.

  • Coordinate with external license partners.

  • Participate in global project meetings.

Document Management

  • Manage document timelines.

  • Ensure on-time document delivery.

  • Maintain document quality standards.

  • Review scientific content for accuracy.

  • Coordinate document reviews and approvals.

  • Provide oversight to internal and external co-authors.

Quality & Compliance

  • Follow Pfizer SOPs.

  • Ensure adherence to global regulatory requirements.

  • Identify compliance risks.

  • Support audit readiness.

  • Maintain inspection-ready documentation.

  • Report deviations when identified.

Scientific Writing

  • Write scientifically accurate safety documents.

  • Summarize complex clinical information.

  • Interpret safety analyses.

  • Maintain clarity and consistency in regulatory documents.

  • Support document strategy development.

Process Improvement

  • Identify workflow improvement opportunities.

  • Recommend process enhancements.

  • Support continuous improvement initiatives.

  • Share best practices across teams.


EDUCATIONAL QUALIFICATIONS

Required

  • Bachelor's Degree in Life Sciences.

Preferred

  • MD

  • PharmD

  • DVM

  • Master's Degree (Life Sciences or related field)

  • PhD


EXPERIENCE REQUIREMENTS

Required

  • Minimum 2 years of experience in:

    • Pharmacovigilance

    • Drug Safety

    • Regulatory Affairs

    • Clinical Research

    • Clinical Trials

    • Medical Writing

Preferred

  • Experience preparing aggregate safety reports.

  • Experience in global pharmacovigilance.

  • Experience with regulatory submissions.