Job ID: 4835
The Research Coordinator facilitates implementation of assigned clinical trials, including data collection and follow-up. Has interpersonal communication skills for interaction with a broad spectrum of health-care disciplines. Performs diverse clinical and clerical duties. Detail oriented and team work skills are required. Must be motivated, organized and be able to function independently. Actively participate in relationships that are equally respectful to all. Willing to work flexible hours and take call with a timely response.
Primary Responsibilities:
- Collaborates with Supervisor to identify all sites and departmental involvement to facilitate appropriate communications/negotiations prior to protocol initiation
- Identifies candidates by screening patient records to maintain consistent enrollment in protocol
- Collaborates with investigators and research team to meet protocol requirements and when necessary seeks clarification, listens and conveys information clearly and correctly in written and verbal form
- Coordinates the collection of data according to the protocol, operations manual and CRFs guidelines and in a timely manner, accurately completes data entry ensuring appropriate legible documentation.
- Demonstrates knowledge of the levels of growth, development and skills for adults and geriatrics
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