Pfizer Hiring Report Coordinator Associate | Apply Now for Pharma Job Opportunities
Looking for a Pharma Job with one of the world’s leading pharmaceutical companies? Pfizer Careers has opened applications for the position of Report Coordinator Associate. This exciting opportunity is ideal for Pharma graduates seeking to build a rewarding career in pharmacovigilance, regulatory reporting, and project management within the pharmaceutical industry.
- Job Title: Report Coordinator Associate
- Locations: Philippines – Makati City, India – Chennai
- Job Requisition ID: 4959140
About the Company
Pfizer is one of the world’s leading biopharmaceutical companies focused on discovering, developing, manufacturing, and delivering innovative medicines and vaccines that improve patient health worldwide. Through continuous innovation and scientific excellence, Pfizer provides career opportunities across clinical research, pharmacovigilance, regulatory affairs, and healthcare operations.
Job Description
- Manage project activities for safety aggregate reports submitted to regulatory bodies like the FDA and EMA.
- Work with teams from Safety, Clinical, Regulatory, and other departments to prepare reports.
- Ensure all reports are completed on time and meet regulatory compliance requirements.
- Coordinate and support smooth collaboration across different functional teams.
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 a document management system.
- Coordinate the review and approval of the report and address review comments.
- Ensure reports are completed before the regulatory due date to meet compliance.
- Guide the 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
- A bachelor’s Degree in the pharmaceutical discipline is required.
- Experience in the pharmaceutical industry, clinical research, or healthcare-related field is preferred.
- 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 is desired.
Technical Skill Requirements
- Experience with: Microsoft Products (e.g., Word, PowerPoint, Excel, Outlook, Teams)
- SharePoint technology
- PDF software (e.g., Adobe)
- Business Objects/Business Intelligence experience is a plus.
