SAE Coordinator - Irving, TX
1 week ago

Job summary
This position is responsible for all serious adverse event (SAE) reporting, SAE record requests, and SAE data entry under the direction and supervision of the Assistant Director of Clinical Trial Management.
Responsibilities
- Provides timely, accurate, and complete submission of SAEs (initial and follow-ups) to the sponsor/or designee by paper form or case report form (CRF).
Job description
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