Clinical Research Coord IApply now (https://secure.dc4.pageuppeople.com/apply/674/gateway/default.aspx?c=apply&lJobID=532547&lJobSourceTypeID=796&sLanguage=en-us) Job no: 532547 Work type: Staff Full-Time Location: Main Campus (Gainesville, FL) Categories: Allied Health, Office/Administrative/Fiscal Support, Grant or Research Administration, Nursing, Health Care Administration/Support Department: 29040100 - MD-ANESTHESIOLOGY-GENERAL Classification Title:Clinical Research Coord IJob Description:The full-time Clinical Research Coordinator l works closely with the Manager of Clinical Research in theDepartment of Anesthesiology and coordinates all aspects of the department’s research component.Serves as study coordinator for research protocols and QA projects as assigned. Activities includerecruiting patients to enroll in studies, providing informed consent, coordinating patient visits, managingpatient visits in accordance with protocol, submitting necessary compliance paperwork, and billingcompliance.Miscellaneous activities include executing tasks as assigned to complete clinical trial(s), satisfying annualcompetencies as required by the University of Florida and Institutional Review Boards, and participating inprofessional development and continuing education.Duties Include:Selects and recruits study participants to enroll in various studies and protocols; participates in theinformed consent process of study subjects; supports the safety of clinical research patients/researchparticipants; coordinates protocol-related research procedures, study visits, and follow-up care; screens,completes case report forms (paper & electronic data capture), and addresses queries.Maintains study source documents; reports adverse events; understands Good Clinical Practice(GCP) and regulatory compliance; educates subjects and family on protocols, study interventions, studydrugs, etc.; complies with institutional policies, standard operating procedures (SOPs), and guidelines.Must comply with federal, state, and sponsor policies and manage essential regulatory documents.Instructs team personnel (nurses, technicians, and students) regarding equipment operation,monitoring procedures, and patient care details associated with clinical studies. Develops in-serviceeducation programs as needed for clinical research.Summarizes conditions of patients and fills out data collection forms, which involves explainingprocedures, protocols, and patient condition to patients and families.Researches regulatory compliance participation in activities to initiate and maintain a currentregulatory file; prepares and submits documents related to research protocols to both internal (UF-IRB,UF-CTC office, UF-OCR, etc.) and external (FDA, WIRB, etc.) organizations as required; completesend-of-study procedures; schedules and participates in sponsored research monitoring visits and QAaudits; ensures the integrity and quality of the research protocol is maintained and the trial is conducted inaccordance with GCP guidelines; attends UF-IRB 01 full board meetings as necessary.Prepares progress reports; periodically reviews study protocols and suggests changes as needed.Reviews research projects periodically to ensure all procedures and aspects comply with nursing standardsand policies. Promotes Human Subjects Protections within clinical research areas.Expected Salary:$44,000 - $49,000Minimum Requirements:Associate’s degree or an allied health professional degree in an appropriate area and one year of relevantexperience; or an equivalent combination of education and experience.Preferred Qualifications: Bachelors Degree Clinical research experience Working understanding of the Epic electronic health record software Working understanding of monitoring study-funded services Ability to collect, collate, analyze, and evaluate data from clinical research studies Ability to work with patients in the perioperative care environment Ability to plan, organize, and coordinate work assignments Ability to work effectively and independently Ability to communicate effectively verbally and in writing Ability to establish and maintain effective working relationships with others Able to multitask when needed; must have excellent time-management skills and be able to effectivelyprioritizeSpecial 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.This is a time limited position.Application must be submitted by 11:55 p.m. (ET) of the posting end date.Health Assessment Required:YesAdvertised: 30 Jul 2024 Eastern Daylight TimeApplications close: 07 Aug 2024 Eastern Daylight Time
