Pfizer, a global leader in healthcare innovation, is hiring an Aggregate Report Analyst Senior Associate in Chennai, India. This role is designed for life sciences professionals passionate about pharmacovigilance, safety writing, and regulatory reporting. If you’re eager to contribute to global drug safety by creating high-quality aggregate reports and risk assessments, this opportunity is for you.
📌 Key Responsibilities
As an Aggregate Report Analyst Senior Associate at Pfizer, you will:
- Prepare safety and regulatory documents including DSURs, PBRERs, RMPs, ACOs, NDA reports, and Canadian Annual Reports.
- Translate complex regulatory requirements into clear, compliant, and timely safety analyses.
- Collaborate with cross-functional teams to ensure accurate data integration and benefit-risk assessment.
- Manage timelines, resources, and vendor deliverables for high-quality document submission.
- Provide oversight to internal or external co-authors when required.
- Continuously identify opportunities for process improvements in safety documentation.
🎓 Qualifications & Experience
- Bachelor’s Degree in Life Sciences with 2+ years relevant experience in patient care, clinical research, safety, or regulatory fields.
- Advanced degrees (MD, DVM, PharmD, Master’s/PhD) are preferred.
- Strong scientific writing, analytical, and regulatory knowledge.
- Ability to synthesize aggregate safety data into structured regulatory documents.
- Basic understanding of medical concepts, disease treatment, and clinical safety principles.
💡 Why Join Pfizer?
- Opportunity to shape global regulatory submissions in a world-class pharmaceutical company.
- Work with a diverse, collaborative global team.
- Gain expertise in pharmacovigilance, aggregate reporting, and regulatory compliance.
- Competitive compensation package with growth opportunities.
💰 Salary Range (Estimated): ₹8,00,000 – ₹14,00,000 per annum (based on experience).
📝 How to Apply
