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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: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

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 aggregate safety reports, benefit-risk assessments, and regulatory safety documents to support clinical development, marketing authorization, and post-marketing pharmacovigilance activities. The role involves analyzing clinical and post-marketing safety data, preparing regulatory submissions, collaborating with global cross-functional teams, and ensuring compliance with ICH, FDA, EMA, and internal regulatory requirements.


KEY RESPONSIBILITIES

Aggregate Safety Reporting

  • Prepare Development Safety Update Reports (DSURs).

  • Prepare Periodic Safety Update Reports (PSURs).

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

  • Develop Addenda to Clinical Overviews (ACOs).

  • Support New Drug Application Periodic Adverse Drug Experience Reports (PADERs).

  • Prepare Risk Management Plans (RMPs).

  • Develop post-marketing safety assessment reports.

Safety Data Analysis

  • Analyze clinical trial safety data.

  • Review post-marketing safety information.

  • Perform integrated safety analyses.

  • Interpret benefit-risk profiles.

  • Identify emerging safety trends.

  • Evaluate pharmacovigilance data.

  • Support regulatory safety assessments.

Scientific & Medical Writing

  • Draft scientifically accurate regulatory documents.

  • Summarize complex clinical and safety data.

  • Develop clear benefit-risk narratives.

  • Prepare responses to regulatory safety queries.

  • Ensure scientific accuracy and consistency across documents.

Regulatory Documentation

  • Prepare global regulatory submission documents.

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

  • Support health authority responses.

  • Maintain regulatory documentation standards.

  • Deliver documents within agreed timelines.

Benefit-Risk Assessment

  • Conduct benefit-risk evaluations.

  • Interpret clinical safety findings.

  • Present evidence-based safety conclusions.

  • Support product safety decision-making.

Cross-Functional Collaboration

  • Collaborate with Worldwide Safety teams.

  • Work with Regulatory Affairs.

  • Coordinate with Medical Affairs.

  • Partner with Clinical Development teams.

  • Collaborate with Epidemiology teams.

  • Support QPPV activities.

  • Coordinate with external license partners.

Quality & Compliance

  • Follow internal SOPs and working procedures.

  • Ensure regulatory compliance.

  • Maintain document quality standards.

  • Support audit and inspection readiness.

  • Identify and report compliance risks.

Project & Document Management

  • Manage document timelines and deliverables.

  • Coordinate with internal and external co-authors.

  • Communicate project status and resource requirements.

  • Support document strategy discussions.

  • Maintain version-controlled documentation.

Process Improvement

  • Identify process improvement opportunities.

  • Recommend workflow 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

  • PhD (Relevant Scientific Discipline)


EXPERIENCE REQUIREMENTS

Required

  • Minimum 2 years of experience in:

    • Pharmacovigilance

    • Drug Safety

    • Clinical Research

    • Clinical Trials

    • Regulatory Affairs

    • Medical Writing

    • Pharmaceutical Industry

    • Patient Care or Clinical Practice

Preferred

  • Experience preparing aggregate safety reports.

  • Experience in global pharmacovigilance.

  • Experience with benefit-risk assessments.

  • Experience with regulatory submissions.