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Report Coordinator Associate

Pfizer
2-5 years
INR 7 LPA – 12 LPA
Chennai, Philippines, United States
1 June 16, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Communication Skills, CPC Certified, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, HCPCS Level II

Report Coordinator Associate

Location: Chennai, India / Makati City, Philippines
Employment Type: Full-Time
Company: Pfizer

Position Summary

The Report Coordinator Associate is responsible for managing the preparation, review, coordination, and submission of safety aggregate reports to global regulatory authorities, including the FDA and EMA. The role works closely with cross-functional teams across Safety, Clinical, Regulatory Affairs, Submissions, and Operations to ensure timely, accurate, and compliant report delivery while maintaining regulatory standards and submission deadlines.

Key Responsibilities

Safety Report Coordination

  • Lead safety aggregate report preparation from planning through regulatory submission.

  • Coordinate report activities with stakeholders from Safety, Clinical, Regulatory, DevOps, and Submission teams.

  • Ensure timely completion of reports in accordance with regulatory requirements.

  • Monitor report timelines and track project milestones.

Data Review & Quality Management

  • Review data and report content for accuracy, completeness, and consistency.

  • Verify alignment of information received from multiple contributors.

  • Support quality review activities to ensure regulatory compliance.

  • Identify and resolve discrepancies in report data.

Document Preparation & Submission

  • Compile and organize report content using electronic document management systems.

  • Coordinate review, approval, and sign-off processes.

  • Address reviewer comments and facilitate report revisions.

  • Ensure final reports are submission-ready before regulatory deadlines.

Stakeholder & Project Management

  • Serve as a central point of coordination among cross-functional teams.

  • Provide guidance regarding report requirements and submission expectations.

  • Support issue resolution and escalation management.

  • Participate in operational and process improvement initiatives.

Systems & Process Support

  • Utilize document management systems and reporting tools effectively.

  • Participate in User Acceptance Testing (UAT) activities when required.

  • Support implementation of new processes, systems, and reporting enhancements.

  • Complete all required Pfizer training and compliance programs.

Educational Qualification

  • Bachelor's Degree in Life Sciences, Pharmacy, Biotechnology, Healthcare, Clinical Research, Nursing, or related discipline.

Experience Required

  • Experience in Pharmaceutical, Clinical Research, Drug Safety, Pharmacovigilance, or Healthcare industry preferred.

  • Exposure to regulatory reporting or safety reporting processes preferred.

  • Experience working in cross-functional project environments.

  • Knowledge of regulatory compliance processes is advantageous.

Technical Skills

  • Safety Aggregate Reporting

  • Pharmacovigilance Operations

  • Regulatory Reporting

  • Clinical Safety Documentation

  • Data Review & Validation

  • Report Coordination

  • Document Management

  • Submission Tracking

  • User Acceptance Testing (UAT)

  • Compliance Management

  • Quality Review

  • Issue Resolution

  • Cross-Functional Coordination

  • Project Management

Software & Systems

  • Microsoft Excel

  • Microsoft Word

  • Microsoft PowerPoint

  • Microsoft Outlook

  • Microsoft Teams

  • SharePoint

  • Adobe Acrobat / PDF Tools

  • Document Management Systems (DMS)

  • Business Objects (Preferred)

  • Business Intelligence Tools (Preferred)

Core Competencies

  • Project Management

  • Attention to Detail

  • Analytical Thinking

  • Communication Skills

  • Stakeholder Management

  • Time Management

  • Organizational Skills

  • Problem Solving

  • Team Collaboration

  • Quality Focus

  • Regulatory Awareness

  • Process Improvement

Preferred Qualifications

  • Experience in Pharmacovigilance or Drug Safety Operations.

  • Understanding of FDA, EMA, and global safety reporting requirements.

  • Knowledge of clinical research and pharmaceutical development processes.

  • Experience with Business Intelligence and reporting tools.

  • Exposure to regulatory compliance frameworks and guidelines.