| Job Description: |
Administrative Responsibilities:
Prepare IRB/ CRC documents etc. for new and ongoing research studies. Maintain regulatory compliance. Collaborate with coordinating centers of various studies. Maintain active collaboration with coordinators and co-investigators, locally, nationally and internationally. Supervise reimbursement process for various research studies. Prepare and update orders, worksheets, checklists etc. Participate in conference calls and attend meetings both on-site and off-site as needed.
Conduct Study Research Visits:
Obtain pertinent information from in a variety of settings for studies. May perform venipuncture, glucose tolerance tests. Coordinate patient-related research data collection and manage sample specimen processing/shipment. Assist in the maintaining of study related supplies and ordering as needed. Maintain accurate patient records.
Recruitment:
The coordinator will independently identify and recruit subjects for research studies across the entire spectrum of the T1D program at UF. Attend camps where necessary, screening events for recruitment and screening purposes. Obtain and arrange transfer of samples from existing Biobanks.
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| Special Instructions to Applicants: |
To be considered for this position, please upload your cover letter or letter of interest, resume, and a list of professional references.
Full-time, Monday through Friday, 08:00 AM to 05:00 PM, with occasional weekend days. May require travel.
The University of Florida is committed to non-discrimination with respect to race, creed, color, religion, age, disability, sex, sexual orientation, gender identity and expression, marital status, national origin, political opinions or affiliations, genetic information and veteran status in all aspects of employment including recruitment, hiring, promotions, transfers, discipline, terminations, wage and salary administration, benefits, and training.
This is a time-limited position.
Application must be submitted by 11:55 p.m. (ET) of the posting end date.
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