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

Clinical Trial Coordinator

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

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