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Responsibilities Triage, Intake, case entry and QC of ICSRs originating from *** 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

The confidential client is seeking a Clinical Trial Consultant II to support pharmacovigilance operations. The role processes and quality-checks clinical trial and post-marketing safety cases, ensuring accurate documentation and compliance with regulatory reporting timelines. Tags Consulting Human Resources Information Technology Insider Connection @Tailored Management 2 email credits available today Beyond your netw