Clinical Research Coord II

Job No: 523650
Work Type: Staff Full-Time
Location: Main Campus (Gainesville, FL)
Categories: Allied Health, Grant or Research Administration
Department: 29051308 - MD-MED QUANTITATIVE HEALTH

Job Description


Classification Title:

Clinical Research Coordinator II

Job Description:

The University of Florida College of Medicine is seeking a Clinical Research Coordinator II for The Intelligent Critical Care Center (IC3). IC3 is a multi-disciplinary center focused on developing and providing sustainable support and leadership for transformative medical Artificial Intelligence (AI) research, education and clinical applications to advance patients' health in critical and acute care medicine. The center addresses an unprecedented opportunity for world-leading, immersive research in AI, the innovation to transform diagnoses, and to monitor and treat critically and acutely ill patients using the multimodal clinical research resources stemming from UF Health, one of Florida's largest health care system. The IC3 is seeking a Clinical Research Coordinator II to assist our transdisciplinary team in conducting cutting-edge clinical research in medical artificial intelligence. Successful applicants will participate in several clinical studies, all part of a large, funded research portfolio that supports several IC3 faculty members. This position is expected to work under the supervision of Faculty and the IC3 Assistant Director of Clinical Research.

Essential Functions

Clinical Research

Screening, collecting, documenting, and maintaining accurate patient study records.

Facilitate daily team communication and participate in regular meetings with the study team or other meetings as necessary. Keep knowledge of research up to date, attend meetings related to research, update training certificates, and access research news and trainings online.

Act as liaison for research subject, investigator, IRB, sponsor, and healthcare professionals.

Document investigational product (drug/device) accountability.

Manage research studies, study subjects, and implementing good clinical practice guidelines.

Identify potential research study participants with the assistance of the Principal Investigator and clinical research staff and recruit them via methods approved by the IRB.

Participates in promoting Human Subjects Protections within clinical research areas.

Administration

Assist as requested in preparation of documents (IRB) required for initial submission to UF research offices. Assist in preparing and submitting regulatory documents for revisions and for continuing review.

Register study in ClinicalTrials.gov database.

Maintains data and filing system of completed ongoing, and pending research protocols.

Manage study finances including sponsor invoicing & resolving study subject billing issues.

Participates in the development and conduct of study billing plans.

Develop informed consent document.

Prepare and compile necessary items for research study visits, such as a participant's event schedule, data collection forms, research equipment, etc.

Develop Case Report Forms.

Expected Salary:

$44,700 - $55,000 - Commensurate with education and experience

Minimum Requirements:

Bachelor's degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.

Preferred Qualifications:

Master's degree in an appropriate area of specialization and 1 year of experience; demonstrated ability to initiate and complete projects with minimal supervision; work effectively and communicate with diverse audiences and interpret technical information and relate it in nontechnical language to local community concerns. A high level of analytical, organizational and planning skills; ability to work independently and as a part of a team; effective oral and written communication skills; ability to interact objectively and effectively with diverse audiences; fluency in computer and communications technology; experience planning and evaluating workshops, trainings and symposia; experience in public outreach/extension. Proficiency in grant writing; willingness to travel, and work occasionally in evenings and weekends.

Special Instructions to Applicants:

"In order to be considered, you must upload your 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.

This requisition has been reposted. Previous applicants are still under consideration and need not apply.

Application must be submitted by 11:55 p.m. (ET) of the posting end date.

Health Assessment Required:
No



Applications Close: 01 Jun 2023

To apply, visit https://explore.jobs.ufl.edu/en-us/job/523650/clinical-research-coord-ii

The University 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.









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