Drug Safety Associate

Pride Global • Stamford, Connecticut, United States • Posted May 16, 2026

About the Role

The Science Team at Russell Tobin is supporting a world-class organization that has an opening for “Drug Safety Associate”



Key Responsibilities

  • Perform end-to-end case processing activities including triage, data entry, and report distribution

  • Assess and process all adverse event case types in compliance with regulatory standards

  • Conduct case triage to determine priority levels when required

  • Identify adverse events, seriousness, and labeledness; evaluate incoming data for reportability

  • Perform coding using MedDRA, WHO-DRUG, and company product dictionaries

  • Identify follow-up requirements and obtain additional information via appropriate channels (email, phone, letters)

  • Conduct quality control (QC) activities, reconciliation, and CRO oversight tasks as needed

  • Manage workload through workflow system...