Responsible for case processing and/or QC of clinical trial ICSRs and post-market case processing from sanctioned countries.
Key Responsibilities:
Triage, Intake, case entry and QC of ICSRs originating from client sponsored studies or other assigned cases
Includes narrative writing, MedDRA coding, drafting of follow-up queries and event notifications to internal stakeholders
Perform retrospective quality checks on processed cases
Independently manage assigned cases, accounting for weekends and holidays, to deliver cases to internal stakeholders on time and ensure case completion ...
Ready to Apply?
Join thousands of Americans building their careers