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Clinical Research Coord IIIApply now (https://secure.dc4.pageuppeople.com/apply/674/gateway/default.aspx?c=apply&lJobID=530165&lJobSourceTypeID=796&sLanguage=en-us) Job no: 530165 Work type: Staff Full-Time Location: Main Campus (Gainesville, FL) Categories: Allied Health, Grant or Research Administration, Health Care Administration/Support Department: 29091800 - MD-PEDS-NEUROLOGY Classification Title:Clinical Research Coord IIIJob Description:Manage research project operations and day-to-day management of the HBCD study. Coordinate and monitor project plans, timelines, and tasks. Communicate with faculty and staff, sponsors, community partners, and other external constituencies as needed, ensuring individuals understand required tasks and monitoring their completion. Organize study meetings, setting agendas, overseeing meeting documentation, and assigning action items/tasks that arise from meetings. Attend national cohort conference calls and follow consortium protocols and directions.Maintain HBCD project compliance with regulations, including creating and renewing IRB protocols, serving as custodian for human subjects' payments, and finalizing any required agreements.Coordinate HBCD project budget preparation, revision, and monitoring. Communicate with the department fiscal team to update budgets as needed. Monitor all HBCD study expenses.Support HBCD-FL staff as needed during participant visits, including collecting data during study visits through questionnaires, placement of biosensors, observations, developmental assessments, and retrieval of electronic medical records, collection of biospecimens and neuroimaging, and general support of participants/families.Assist with preparation of HBCD progress reports, summarizing study activities, creating budget justifications, and formatting NIH-required documents.Expected Salary:$52,000.00 - $70,00.00Minimum Requirements:Bachelor's degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience.Preferred Qualifications:

Masters Degree, PhD, RN, or similar credential in a health related field.

The ideal candidate will have one or more years of experience as a Clinical Research Coordinator II or equivalent. This position requires knowledge of current clinical research best practices and experience in compliance with human subject IRB practices.

Excellent interpersonal skills, integrity and dependability; curiosity, adaptability, and optimism; superior organizational skills and attention to detail; creativity and critical thinking skills; and a strong work ethic.

Experience conducting research among diverse populations, including patient recruitment, data collection, and promotion of retention in longitudinal studies.

Advanced computer skills using MS Word, Excel, and PowerPoint.

Experience working with electronic data capture systems such as REDCap.

Excellent written & oral communication.

Ability to work independently and able to work collaboratively, with the ability to problem solve independently, forwarding issues and ideas to the team and/or leadership as appropriate.

Coursework and/or experience in budgeting.

Experience in project management.

Special Instructions to Applicants:In order to be considered, you must upload your cover letter and resume.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.Application must be submitted by 11:55 p.m. (ET) of the posting end date.Health Assessment Required:YesAdvertised: 31 Jan 2024 Eastern Standard TimeApplications close: 07 Feb 2024 Eastern Standard Time

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