Fortrea – Safety Science Specialist, Clinical Research Candidates Apply Now
Are you a detail-oriented and experienced safety professional with 3-4 years of experience in the pharmaceutical industry? Fortrea, a leading company dedicated to providing high-quality safety and clinical services, is seeking a dedicated Safety Science Specialist to join our team in Bangalore. If you are passionate about ensuring the highest standards of safety and quality in clinical trials and post-marketing settings, we encourage you to apply! This is a full-time position.
Job Title: Safety Science Specialist
Location: Bangalore
Job Type: Full-time
Posted On: Posted Today
End Date to Apply: April 16, 2025 (11 hours left to apply)
Job Requisition ID: 25684
Job Overview
-
Assist in the overall Clinical Safety and/or Pharmacovigilance Safety Surveillance (PSS) operations related to assigned products.
-
Handle all aspects of the adverse events (AEs) process, including those from clinical trials and post-marketing settings (e.g., unsolicited reports).
-
Manage and process expeditable adverse events (serious and unexpected AEs) according to required standard.
Summary of Responsibilities:
As a Safety Science Specialist at Fortrea, your responsibilities will include:
- Data entry of safety data onto adverse event database(s) and tracking systems.
- Review of adverse events for completeness, accuracy, and appropriateness for expedited reporting.
- Writing patient narratives and coding adverse events accurately using MedDRA.
- Determining listedness against appropriate label for Marketed products, if applicable.
- Identifying clinically significant information missing from the reports and ensuring its collection.
Qualifications (Minimum Required):
- 3 to 4 years of safety experience
Keywords: Safety Science Specialist, Fortrea, Bangalore, Drug Safety, Pharmacovigilance, Adverse Events, Clinical Trials, Post-Marketing, Safety Data, MedDRA, Pharmaceutical, Healthcare, Safety Management, Regulatory Reporting.
