Exciting Pfizer Hiring Report Coordinator Associate
Urgent Pfizer Hiring Report Coordinator Associate | Life Sciences Apply
Pfizer is hiring for the position of Report Coordinator Associate in Chennai under a hybrid work model. This opportunity is ideal for candidates from Life Sciences, Pharmacy, Clinical Research, Healthcare, and Pharmaceutical backgrounds who are interested in drug safety reporting, regulatory compliance, aggregate safety reports, project coordination, and pharmacovigilance operations.
The selected candidate will support the preparation, coordination, review, and submission of aggregate safety reports for global regulatory agencies, including the FDA and EMA. This role offers excellent exposure to pharmacovigilance, regulatory affairs, safety reporting, clinical research operations, and global drug development programs.
Company Overview
Pfizer is one of the world’s leading biopharmaceutical companies dedicated to discovering, developing, and delivering innovative medicines and vaccines. With a strong global presence, Pfizer continues to advance healthcare through scientific innovation, research excellence, and patient-focused solutions.
The company provides professionals with opportunities to contribute to global clinical development, regulatory compliance, drug safety monitoring, and healthcare innovation programs.
Job Role & Responsibilities
Safety Report Coordination
- Coordinate preparation and submission of aggregate safety reports.
- Manage report timelines from planning through final submission.
- Ensure reports meet regulatory submission deadlines.
- Support compliance with global regulatory requirements.
Project Management Activities
- Lead report preparation activities with key stakeholders.
- Coordinate across Safety, Clinical, Regulatory, Development Operations, and Submission teams.
- Monitor project milestones and deliverables.
- Resolve issues affecting report completion timelines.
Data Review & Quality Control
- Review safety data for consistency and accuracy.
- Verify information received from various contributors.
- Ensure quality and completeness of regulatory reports.
- Support compliance with internal quality standards.
Documentation & Submission Support
- Compile report content using electronic tools and document management systems.
- Coordinate review and approval workflows.
- Address review comments and stakeholder feedback.
- Support regulatory submission readiness activities.
Regulatory Compliance
- Ensure reports comply with FDA, EMA, and global regulatory requirements.
- Support pharmacovigilance and drug safety reporting processes.
- Maintain compliance with company SOPs and regulatory guidelines.
- Participate in compliance and quality improvement initiatives.
System & Process Support
- Support User Acceptance Testing (UAT) activities when required.
- Participate in process improvement projects.
- Complete assigned training and compliance requirements.
- Contribute to operational excellence initiatives.
Eligibility / Qualifications
Educational Qualification
Candidates must possess:
- Bachelor’s Degree in Life Sciences
- Bachelor’s Degree in Healthcare
- Bachelor’s Degree in Pharmacy
- Bachelor’s Degree in Pharmaceutical Sciences
- Related Healthcare Disciplines
Eligible Courses
B.Pharm, M.Pharm, Pharm D, B.Sc Life Sciences, M.Sc Life Sciences, B.Sc Biotechnology, M.Sc Biotechnology, B.Sc Microbiology, M.Sc Microbiology, B.Sc Biochemistry, M.Sc Biochemistry, Clinical Research, Biomedical Sciences, Public Health, Healthcare Management, Pharmaceutical Sciences, and related disciplines.
Experience Required
- Experience in pharmaceutical industry, clinical research, healthcare, pharmacovigilance, or regulatory operations is preferred.
- Freshers with strong academic backgrounds and relevant internships may also be considered depending on business requirements.
Required Skills
Pharmacovigilance & Regulatory Skills
- Aggregate Safety Reporting
- Pharmacovigilance Operations
- Drug Safety Reporting
- Regulatory Compliance
- Safety Documentation
- Global Regulatory Requirements
Project Management Skills
- Project Coordination
- Timeline Management
- Stakeholder Management
- Issue Resolution
- Cross-Functional Collaboration
- Workflow Management
Technical Skills
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
- Microsoft Outlook
- Microsoft Teams
- SharePoint
- Adobe PDF Tools
Preferred Technical Knowledge
- Business Objects
- Business Intelligence Tools
- Safety Reporting Systems
- Document Management Systems
Professional Skills
- Excellent Communication Skills
- Presentation Skills
- Attention to Detail
- Problem Solving
- Organizational Skills
- Team Collaboration
Location & Salary
Location: Chennai, Tamil Nadu
Work Model: Hybrid
Salary: ₹5.5 LPA – ₹9 LPA (Approximate Industry Standard Based on Experience and Industry Background)
Why Join Pfizer?
- Opportunity to work with a globally recognized pharmaceutical leader.
- Exposure to global pharmacovigilance and regulatory reporting activities.
- Career growth in drug safety, regulatory affairs, and clinical operations.
- Hybrid work environment.
- Strong learning and development opportunities.
- Experience working with FDA and EMA regulatory submissions.
Application Process
Interested candidates can apply through the official Pfizer Careers portal.
Frequently Asked Questions (FAQs)
1. What qualification is required for the Report Coordinator Associate role?
Candidates with degrees in Pharmacy, Life Sciences, Healthcare, Pharmaceutical Sciences, and related disciplines are eligible.
2. Is prior pharmacovigilance experience mandatory?
No. However, experience in pharmaceutical, clinical research, healthcare, regulatory affairs, or drug safety functions is preferred.
3. What are aggregate safety reports?
Aggregate safety reports are regulatory documents that summarize safety information for pharmaceutical products and are submitted to agencies such as the FDA and EMA.
4. What technical skills are required?
Candidates should be proficient in Microsoft Office applications, SharePoint, Adobe PDF tools, and document management systems.
5. Is this a hybrid role?
Yes. The position follows a hybrid work model.
6. Where is the job located?
The role is based in Chennai, India.
Job Summary
| Category | Details |
|---|---|
| Company | Pfizer |
| Department Vacancies | Report Coordinator Associate |
| Qualification | B.Pharm, M.Pharm, Pharm D, Life Sciences, Healthcare, Pharmaceutical Sciences |
| Experience | Pharmaceutical, Clinical Research, Healthcare or Regulatory Experience Preferred |
| Location | Chennai |
To apply for this job please visit pfizer.wd1.myworkdayjobs.com.
