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...