Life Science Jobs | Pfizer is Hiring an Associate | Apply Now
Looking to step into global life science jobs with one of the world’s most trusted pharmaceutical companies? Pfizer is hiring for an Associate – Aggregate Report Coordinator in Chennai. This role offers an exciting opportunity to work at the intersection of pharmacovigilance, regulatory compliance, and clinical safety, making it an ideal associate job for candidates aiming to grow their Pfizer career in drug safety and aggregate reporting.
Job Details
- Job Title: Associate – Aggregate Report Coordinator
- Location: India – Chennai
- Job Type: Full time
- Job Requisition ID: 4949842
About the Company
Pfizer is a globally recognized biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that significantly improve patient health. With a strong presence in India, Pfizer offers diverse life science jobs across research, safety, and regulatory domains. The company emphasizes scientific excellence, regulatory compliance, and patient safety in all its operations. Pfizer fosters a collaborative, inclusive, and ethical work culture that supports continuous learning and career growth. Professionals pursuing a long-term Pfizer career benefit from exposure to global projects and cross-functional teams. Pfizer remains an employer of choice for impactful associate jobs in the life sciences sector.
Key Responsibilities
- Lead report preparation from prep to submission with key stakeholders/contributors within Clinical, Regulatory, Safety, DevOps, Submissions, etc.
- Review data to ensure consistency between various contributors.
- Compile the information for reports using various electronic tools and document management system.
- Coordinate the review and approval of the report and address review comments.
- Ensure reports are completed prior to regulatory due date to meet compliance.
- Provide guidance to contributor regarding report requirements.
- Participate in projects or subject matter tasks that support the group and deliverables.
- Participate in developing and performing User Acceptance Testing (UAT) as required.
- Complete training in accordance with Pfizer’s and WSR Safety information Management curriculum.
Qualifications
- Bachelor’s Degree in life sciences
Technical Skills
- Experience in the pharmaceutical industry, clinical research, or healthcare related field.
- Experience with Microsoft Word & Excel, Adobe Acrobat, ISI Toolbox, etc.
- Experience with SharePoint technology (e.g., Microsoft InfoPath, SharePoint Designer, etc.)
- Business Objects experience is a plus.
Skills
- Excellent English verbal, written communication and presentation skills required.
- Must be detail-oriented.
- Strong project management and issue resolution skills required.
- Demonstrated ability to perform in a cross-functional environment.
- Knowledge of regulatory/safety regulations and guidelines desired.
This is a high-impact associate job for professionals aiming to build a meaningful Pfizer career in pharmacovigilance and regulatory safety. If you aspire to contribute to global drug safety while advancing your role in life science jobs, this opportunity at Pfizer is your next strategic career move.
