Pfizer Hiring For Pharmacovigilance Aggregate Report Coordinator

Pfizer, a global leader in biopharmaceutical innovation, is inviting applications for the position of Associate – Aggregate Report Coordinator at its Chennai, India location. This role is ideal for professionals with experience in pharmacovigilance, safety aggregate reporting, regulatory compliance, and cross-functional project coordination within the pharmaceutical or clinical research domain.

The Associate Aggregate Report Coordinator will play a critical role in managing and delivering regulatory safety aggregate reports submitted to global health authorities such as the FDA and EMA, ensuring compliance with international safety regulations and timelines.

Key Responsibilities – Aggregate Report Coordinator Role

• Lead end-to-end safety aggregate report preparation, from planning to regulatory submission
• Collaborate with Clinical, Regulatory Affairs, Safety, DevOps, and Submissions teams
• Review and validate data for accuracy, consistency, and regulatory compliance
• Compile reports using electronic authoring tools and document management systems
• Coordinate cross-functional reviews, manage approvals, and resolve reviewer comments
• Ensure on-time submission of aggregate reports to meet global regulatory deadlines
• Provide guidance to contributors on aggregate report requirements and standards
• Participate in process improvement initiatives, special projects, and UAT activities
• Complete all required training under Pfizer’s Safety Information Management curriculum

Required Qualifications & Skills

Educational Qualifications

• Bachelor’s Degree in Life Sciences, Pharmacy, Healthcare, or a related discipline (mandatory)

Experience & Technical Skills

• Experience in the pharmaceutical industry, pharmacovigilance, clinical research, or healthcare
• Strong working knowledge of:
  • Microsoft Word & Excel
  • Adobe Acrobat
  • ISI Toolbox
  • SharePoint technologies (InfoPath, SharePoint Designer)
• Business Objects experience is an added advantage

Core Competencies

• Excellent English verbal and written communication skills
• High level of attention to detail and data accuracy
• Strong project management and issue resolution capabilities
• Proven ability to work in a cross-functional, global environment
• Knowledge of global safety and regulatory guidelines (ICH, FDA, EMA preferred)

Why Join Pfizer?

• Work with a globally respected pharmaceutical organization
• Exposure to international pharmacovigilance and regulatory reporting
• Hybrid work model supporting work–life balance
• Strong emphasis on training, compliance, and career development
• Equal opportunity employer with a culture of inclusion and innovation

How to Apply

Application Link