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Pfizer
Pfizer Recruitment 2026 – Report Coordinator Associate
Pfizer, one of the world’s leading biopharmaceutical companies, is inviting applications for the position of Report Coordinator Associate. This opportunity is available in Chennai, India and Makati City, Philippines under a hybrid work model. Candidates with a background in life sciences, healthcare, or pharmaceuticals are encouraged to apply.
Job Details
- Company: Pfizer
- Position: Report Coordinator Associate
- Location: Chennai, India / Makati City, Philippines
- Job Type: Full-Time
- Work Mode: Hybrid
- Qualification: Bachelor’s Degree in Life Sciences, Healthcare, or Pharmaceutical Discipline
- Experience: Preferred experience in the pharmaceutical industry, clinical research, or healthcare-related field
About the Role
The Report Coordinator Associate will be responsible for the project management and coordination of safety aggregate reports submitted to global regulatory authorities, including the FDA and EMA. The role involves working closely with cross-functional teams from Safety, Clinical, Regulatory Affairs, Submissions, and other departments to ensure timely and compliant report submissions.
Key Responsibilities
- Lead safety aggregate report preparation from initiation to final submission.
- Coordinate with stakeholders from Clinical, Regulatory, Safety, DevOps, and Submissions teams.
- Review data and ensure consistency across multiple contributors.
- Compile and manage report content using electronic tools and document management systems.
- Coordinate review and approval workflows while addressing reviewer comments.
- Ensure all reports are completed and submitted before regulatory deadlines.
- Provide guidance to contributors regarding report requirements and compliance expectations.
- Participate in process improvement initiatives, projects, and subject matter activities.
- Support User Acceptance Testing (UAT) activities when required.
- Complete mandatory training programs as per Pfizer’s Safety Information Management curriculum.
Required Technical Skills
Candidates should have experience with:
- Microsoft Word, Excel, PowerPoint, Outlook, and Teams
- SharePoint Technology
- PDF Software (Adobe Acrobat or similar)
Preferred Skills
- Business Objects / Business Intelligence experience
- Knowledge of regulatory and drug safety guidelines
- Strong project management and issue resolution skills
- Excellent verbal and written English communication skills
- Ability to work effectively in a cross-functional environment
- Strong attention to detail and organizational skills
Educational Qualification
- Bachelor’s Degree in Life Sciences, Healthcare, Pharmacy, or related Pharmaceutical Discipline.
Why Join Pfizer?
Pfizer offers an opportunity to work on globally significant drug safety and regulatory compliance projects while collaborating with international teams. Employees gain exposure to global pharmacovigilance processes, regulatory reporting standards, and career growth opportunities within one of the most respected pharmaceutical organizations worldwide.
How to Apply
Interested and eligible candidates can apply online through Pfizer’s official careers portal. Applications are reviewed on a rolling basis, so early application is recommended.
Apply Now and become part of Pfizer’s mission to deliver breakthroughs that change patients’ lives.
APPLY HERE
To apply for this job please visit pfizer.wd1.myworkdayjobs.com.
