Clinical Research Associate- Contingent- Day Shift (8:15-6:30p)

General hours 10am - 7pm, however when C sections are scheduled, the shift may begin as early as 07:15 am Monday-Friday, Saturdays are approximately 3 hours, one Saturday a month**
General Summary
Participates in the design, administration and monitoring of clinical trials.
Responsibilities
Plans, organizes, performs and monitors daily project protocols.
Collects, prepares and maintains required research documentation, such as informed consent records, case records, clinical notes and medical reports.
Reports and assists with the management of protocol deviations, adverse events and other project-related issues.
Assists with the preparation and delivery of internal and external presentations, conference reports and lectures, and publishing submissions.
Understanding of the Food and Drug Administration (FDA) rules is beneficial.
Education/Experience Required
High School diploma equivalency with 2 years of cumulative experience OR Associate degree/Technical degree OR 4 years of applicable cumulative job specific experience required.
Some college work and phlebotomy experience or equivalent is preferred
Work dedicated to Birthing Center patients is preferred