Description This is a full-time/non-exempt term position lasting six months to one year. JOB SUMMARY: Supports the activities of the Principal Investigator in accordance with the protocols and regulations. Involved in the collection, interpretation and documentation of data in support of clinical trials. Conducts off-site audits. Initiates and develops process improvements. Trains and mentors new staff members. KEY RESPONSIBILITIES: Coordinate protocol and patient consent form process. Coordinates preparation of all IRB and regulatory documents; under direction of PI may draft various communications with Sponsor. Develops assessment tool pre protocol to use in clinica
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