What are the responsibilities and job description for the Clinical Research Associate- Contingent- Day Shift (8:15-6:30p) position at CHEManager International?
- 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.
- 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