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Clinical Research Coordinator
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$40 - $44 an hour
- JOB DESCRIPTION Description:Experience Requirements: Bachelor’s Degree required with 4-6 years experience
- Prepare, submit and track regulatory documentation, including informed consents, for activation, maintenance, amendments and close-out
- Review IRB approved documents for accuracy; file such documents and communicate with all key stakeholders regarding IRB determinations
- Draft and submit essential reports to the appropriate IRB such as IND safety reports, AEs/SAEs, deviations, ADEERS submissions, consent form changes, etc.
- This position requires Ophthalmology experience.
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