Regulatory Affairs Coordinator

4 weeks ago


Chennai, Tamil Nadu, India Pfizer Full time

Position Overview

We are seeking a highly skilled Regulatory Affairs Coordinator to join our team at Pfizer.

Key Responsibilities

  1. Lead the preparation of safety aggregate reports from submission to completion.
  2. Collaborate with cross-functional teams to ensure compliance with regulatory requirements.
  3. Review data for consistency and accuracy.
  4. Compile information using various electronic tools and document management systems.
  5. Coordinate review and approval of reports.
  6. Ensure timely completion of reports to meet regulatory deadlines.
  7. Develop and perform User Acceptance Testing (UAT) as required.
  8. Complete training in accordance with Pfizer's and WSR Safety information Management curriculum.

Requirements

  • Experience in the pharmaceutical industry, clinical research, or healthcare.
  • Proficiency in Microsoft Office, Adobe Acrobat, and SharePoint technology.
  • Business Objects experience is a plus.
  • Bachelor's Degree in life sciences, healthcare, or pharmaceutical discipline.
  • Excellent English communication and presentation skills.
  • Detail-oriented and strong project management skills.

About Pfizer

Pfizer is an equal opportunity employer committed to diversity and inclusion.



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