Job ID: 14627
GENERAL SUMMARY:
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.
PREFERRED KNOWLEDGE AND SKILLS:
- Venipuncture certification within 3 months of hire
- Read and interpret medical records
- Basic ECG reading skills
EDUCATION AND EXPERIENCE REQUIRED:
- Experienced Licensed Registered Nurse
- Cardiology or Critical Care experience
- CPR
PREFERRED EDUCATION AND EXPERIENCE:
- Bachelor Degree
- Previous Research Experience
- Cath Lab or CV Surgical Experience
LICENSURE, CERTIFICATION, OR REGISTRATION REQUIRED:
- Registered Nurse
PRINCIPAL DUTIES AND JOB RESPONSIBILITIES:
- Demonstrates through behavior Florida Hospital’s core values of Integrity, Care, Balance, Excellence, Stewardship, and Teamwork as outlined in the organization’s Performance Excellence Program booklet.
- 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 protocols.
- Ensure that patients are provided informed consent to participate in a clinical trial.
- 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.
- Conducts trials according to FDA, IRB and protocol guidelines
- Maintains complete and accurate communications/source documentation
- Schedules and participates in monitor visits and /or audits as required for each trial in a timely and professional manner
- Manages time efficiently and communicates effectively and frequently with research team members.
- Is flexible with working schedule and willing to travel to other campuses, offices or meetings when necessary.
- Demonstrates knowledge of the levels of growth, development and skills for adults
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