The Drug Safety Associate will be responsible for processing and oversight of (AE) adverse event/drug experience reports (serious and non-serious) and other safety-related data for Incite marketed products and clinical trials. The position will be responsible for the case management life cycle from receipt through case completion.
Completion of the case management life cycle including but not limited to: intake, triage, book-in, data entry, peer/quality review, follow-up, and submissions.
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