NewClinical Research Coordinator I - Pediatrics CHRI Pediatrics CHRIClinical Research Coordinator I - Pediatrics CHRIGainesville, FloridaThe Clinical Research Coordinator I must be able to perform the following essential functions independently: Coordinate clinical research studies Activities include and are not limited to: recruiting patients to enroll in study(ies); coordinating patient visits; managing patient visits in accordance to protocol; coordinating site monitor visits; submitting necessary compliance paperwork; ensuring billing compliance; resolving issues/questions with the sponsor; serving as the liaison between the Principal Investigator and study subjects; performing study feasibility assessments for potential new studies. Activities included but are not limited to: initiating and maintaining a current regulatory file; preparing and submitting documents related to clinical trials to both internal (UF-IRB, UF-OCR, UF-IBC, etc.) and external (FDA, RAC,WCG, etc) organizations as required; completing end of study procedures; scheduling and participating in sponsored research monitoring visits; assuring that the clinical research trial's integrity and quality are maintained and that the trial is conducted following Good Clinical Practice guidelines; attending UF-IRB 01 full board meetings as necessary.
NewClinical Research Coordinator I - Pediatrics CHRI University of FloridaClinical Research Coordinator I - Pediatrics CHRIGainesville, FL$46,000–$50,000 / yearThe Clinical Research Coordinator I must be able to perform the following essential functions independently: Coordinate clinical research studies Activities include and are not limited to: recruiting patients to enroll in study(ies); coordinating patient visits; managing patient visits in accordance to protocol; coordinating site monitor visits; submitting necessary compliance paperwork; ensuring billing compliance; resolving issues/questions with the sponsor; serving as the liaison between the Principal Investigator and study subjects; performing study feasibility assessments for potential new studies. Activities included but are not limited to: initiating and maintaining a current regulatory file; preparing and submitting documents related to clinical trials to both internal (UF-IRB, UF-OCR, UF-IBC, etc.) and external (FDA, RAC,WCG, etc) organizations as required; completing end of study procedures; scheduling and participating in sponsored research monitoring visits; assuring that the clinical research trial's integrity and quality are maintained and that the trial is conducted following Good Clinical Practice guidelines; attending UF-IRB 01 full board meetings as necessary.
Clinical Research Coordinator III University of FloridaClinical Research Coordinator IIIGainesville, FL$60,000–$82,000 / yearThe Clinical Research Coordinator III must be able to perform the following essential just functions independently for multiple ongoing clinical trials: Serve as study coordinator for clinical trial protocols as assigned: Activities include and are not limited to: recruiting patients to enroll in study(ies); coordinating patient visits; managing patient visits in accordance to protocol; coordinating site monitor visits; submitting necessary compliance paperwork; ensuring billing compliance; resolving issues/questions with the sponsor; serving as the liaison between the Principal Investigator and study subjects; performing study feasibility assessments for potential new studies. Clinical trial regulatory compliance management: Activities included but are not limited to: initiating and maintaining a current regulatory file; preparing and submitting documents related to clinical trials to both internal (UF-IRB, UF-OCR, UF-IBC, etc.) and external (FDA, RAC, WIRB, etc) organizations as required; completing end of study procedures; scheduling and participating in sponsored research monitoring visits; assuring that the clinical research trial''''s integrity and quality are maintained and that the trial is conducted following Good Clinical Practice guidelines; attending UF-IRB 01 full board meetings as necessary.
NewClinical Research Coordinator III - Pediatric Endocrinology University of FloridaClinical Research Coordinator III - Pediatric EndocrinologyGainesville, FL$65,000–$75,000 / yearAdministrative/Compliance Responsibilities: Prepare IRB, CRC, and RAC documents for new and ongoing research studies, assess study feasibility, prepare study budgets, prepare and negotiate study contracts, maintain regulatory binders, supervise reimbursement processes, perform internal audits, and mentor junior coordinators. Oversee the timely scheduling of subjects in the clinical research center (CRC), obtain informed consent, and ensure adherence to study protocol (both nursing staff and patients and their families), and specimen processing/shipment.
Clinical Research Coordinator II - UF Emergency Medicine University of FloridaClinical Research Coordinator II - UF Emergency MedicineGainesville, FL$53,000–$60,000 / yearThe Clinical Research Coordinator II will work collaboratively with the Vice Chair of Research, Principal Investigators (PIs), the Clinical Research Manager, research administrators, coordinators, sponsors, and institutional partners to ensure all research activities are conducted in accordance with federal regulations, University of Florida policies, and sponsor requirements. This position plays a vital role in coordinating and managing clinical research activities across all phases of study operations, including regulatory submissions, participant recruitment and enrollment, study implementation, data collection, compliance monitoring, reporting, and project closeout.
Clinical Research Coordinator II - Pediatric Endocrinology University of FloridaClinical Research Coordinator II - Pediatric EndocrinologyGainesville, FloridaClinical Research Coordination: Responsible for coordinating a large, multi-site project planning, serving as a liaison for research subjects and participating health centers for the investigator, IRB, sponsor and other healthcare professionals, recruiting study participants, and extensive data collection including survey and focus group data. This individual will work in a team setting monitoring and, under the supervision of the Principal Investigators, will be involved in coordinating project planning, serving as a liaison for research subjects and participating health centers for the investigator, IRB, sponsor and other healthcare professionals.
NewClinical Research Analyst I - Clinical Research Hub University of FloridaClinical Research Analyst I - Clinical Research HubGainesville, FloridaThe Analyst will be responsible for assisting in building protocols in UF’s Clinical Trials Management System (CTMS) for the Academic Health Center’s (AHC) and the Oncology (ONC) human subject clinical research projects under the purview of CRH. The professional knowledge and expertise required includes but is not limited to proficiency in the CTMS or similar research software, proficiency in Microsoft Office (Excel, Word, and Outlook), general knowledge of Clinical Trials.
Clinical Research Coord I University of FloridaClinical Research Coord IGainesville, FL$46,000–$53,000 / yearAs part of an interdisciplinary health team, the incumbent will collaborate with other CRCs, physicians, nurses, and other key personnel in the department and clinic to ensure compliance with protocol requirements and satisfactory care for enrolled patients. As part of an interdisciplinary health team, the incumbent will collaborate with other CRCs, physicians,nurses, and other key personnel in the department and clinic to ensure compliance with protocol requirements and satisfactory care for enrolled patients.
NewClinical Research Coord II University of FloridaClinical Research Coord IIGainesville, FL$53,000–$57,000 / yearResearches regulatory compliance participation in activities to initiate and maintain a current regulatory 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; completes end-of-study procedures; schedules and participates in sponsored research monitoring visits and QA audits; ensures the integrity and quality of the research protocol is maintained and the trial is conducted in accordance with GCP guidelines; attends UF-IRB 01 full board meetings as necessary. Selects and recruits study participants to enroll in various studies and protocols; participates in the informed consent process of study subjects; supports the safety of clinical research patients/research participants; coordinates protocol-related research procedures, study visits, and follow-up care; screens, completes case report forms (paper & electronic data capture), and addresses queries.
Clinical Research Assistant-Department of Neurosurgery-RNA Lab University of FloridaClinical Research Assistant-Department of Neurosurgery-RNA LabGainesville, FL$19.32–$21.89 / hourTo claim veterans'''' preference, indicate the claim on the application and provide required documentation by uploading a DD-214 (or equivalent certification from the Department of Veteran Affairs) and any additional supporting documentation based on the type of claim. Under the direction of the Research and Development Manager, PIs, and Clinical Veterinary Oncologists, prepares new study requests and protocol/consent modifications to be sent to the IACUC and VHHRC.
Research Nurse / Study Coordinator II University of FloridaResearch Nurse / Study Coordinator IIGainesville, FL$60,000–$67,500 / yearAs a Study Coordinator II / Research Nurse at the UF Health Cancer Institute (UFHCI), you will be responsible for collaborating with coordinators and research staff, investigators, physicians, nurses, and other key personnel in the clinics, hospitals, and at the Cancer Center to ensure compliance with protocol requirements and satisfactory care for patients enrolled on research protocols. As a matrix cancer center, we span all of the University of Florida''''s 16 colleges, pulling together a world-class, multi-disciplinary membership of over 350 faculty and 150 staff to address the challenges of the cancer burden faced by the population we serve as we work together to find a cure.
NewCoordinator Clinical | Clinical Decision Unit | Full Time | Variable University of Florida Health Science CenterCoordinator Clinical | Clinical Decision Unit | Full Time | VariableGainesville, FLMotor Vehicle Operator Designation: Employees in this position: Will not operate vehicles for an assigned business purpose NOTE: A frequent driver is defined as one who uses his/her personal or Shands automobile a) at least once daily, b) at least five individual trips per week or c) drives, on average, over 150 miles per week in the performance of his/her job. Accountable for daily staffing and unit-based follow-up of issues that assist in the assessment, planning, implementation and evaluation of patient care needs based on quality benchmarking, patient acuity/care trends, staff clinical education needs and patient satisfaction.
NewCoordinator Clinical | Clinical Decision Unit | Full Time | Variable UF HealthCoordinator Clinical | Clinical Decision Unit | Full Time | VariableGainesville, FloridaFull timeMotor Vehicle Operator Designation: Employees in this position: Will not operate vehicles for an assigned business purpose NOTE: A frequent driver is defined as one who uses his/her personal or Shands automobile a) at least once daily, b) at least five individual trips per week or c) drives, on average, over 150 miles per week in the performance of his/her job. Accountable for daily staffing and unit-based follow-up of issues that assist in the assessment, planning, implementation and evaluation of patient care needs based on quality benchmarking, patient acuity/care trends, staff clinical education needs and patient satisfaction.
Research Coordinator II - Infectious Diseases University of FloridaResearch Coordinator II - Infectious DiseasesGainesville, FL$46,000–$55,000 / yearDuties for this position, which is based in Gainesville, include laboratory management (including purchasing, maintaining regulatory documents, ensuring biohazard and biosafety complains, and supervising undergraduate students) as well as coordination of clinic studies (including filing regulatory documents with the IRB, maintaining paper and electronic data capture, conducting surveys, development and maintaining research RedCap databases, auditing databases and summarizing reports). Laboratory Management & Research Activities: Laboratory management (including biohazard, biosafety matters and student oversight) and conducting laboratory assays (viral and bacterial diagnostic serological assays, cell culture maintenance, molecular work (RT-qPCRs, preparing samples for sequencing).
OPS - Research Coordinator - College of Nursing University of FloridaOPS - Research Coordinator - College of NursingGainesville, FL$23–$24 / hourThis position plays a key role in coordinating study operations, engaging with participants and healthcare teams, and ensuring high‑quality data collection and regulatory compliance. Job Description: The University of Florida College of Nursing is seeking a motivated and detail‑oriented OPS Research Coordinator to support ongoing clinical and health services research activities.
OPS - Research Coordinator - College of Nursing College of NursingOPS - Research Coordinator - College of NursingGainesville, FloridaThis position plays a key role in coordinating study operations, engaging with participants and healthcare teams, and ensuring high‑quality data collection and regulatory compliance. Job Description: The University of Florida College of Nursing is seeking a motivated and detail‑oriented OPS Research Coordinator to support ongoing clinical and health services research activities.
Couples & Relationship Coordinator & Clinical AST/ASO Professor University of FloridaCouples & Relationship Coordinator & Clinical AST/ASO ProfessorGainesville, FLThe clinical associate/assistant professor and Couples & Relationship Coordinator’s primary responsibility is to provide direct clinical services (e.g., group, individual and couples counseling) to University of Florida students; as well as coordinate the couples counseling program at the CWC, including clinical services and training program elements. In addition to experience with couples & relationship counseling, the successful candidate should have experience in one or more of the following areas related to collegiate mental health: assessment/psychological testing, neurodivergence, alcohol & other drug use, trauma, disordered eating concerns, attention-deficit/hyperactivity disorders, and/or psychotherapy and outreach with students from a range of identities/cultural backgrounds.
NewClinical Research Nurse Navigator-Department of Neurosurgery-Neuro-Oncology University of FloridaClinical Research Nurse Navigator-Department of Neurosurgery-Neuro-OncologyGainesville, FloridaServe as a clinical nursing resource for patients, families, healthcare providers, advocacy organizations, and community partners regarding brain tumor treatment, clinical research, and available resources. •Collaborate with physicians, advanced practice providers, clinical research coordinators, social workers, and multidisciplinary care teams to address barriers to participation and optimize patient outcomes.
Clinical Programs Coordinator II - Pediatric Endocrinology University of FloridaClinical Programs Coordinator II - Pediatric EndocrinologyGainesville, FL$63,000–$70,000 / yearTravel and program development: Coordinate statewide diabetes screening and outreach activities in collaboration with UF faculty, state agencies, and community organizations. Classification Minimum Requirements: Bachelor''''s degree in in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.
Study Coordinator I/II University of FloridaStudy Coordinator I/IIGainesville, FL$48,000–$55,000 / yearAs a Study Coordinator at the UF Health Cancer Institute (UFHCI), you will be responsible for collaborating with coordinators and research staff, investigators, physicians, nurses, and other key personnel in the clinics, hospitals, and the Cancer Institute to ensure compliance with protocol requirements and satisfactory care for patients enrolled on research protocols. Classification Title: Clinical Research Coordinator I/II Classification Minimum Requirements: Clinical Research Coordinator I: Associate''''s degree or an allied health professional degree in an appropriate area and one year of relevant experience; or an equivalent combination of education and experience.