Clinical Research Coord III
Clinical Research Coord III
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
$ 65000 - 76500
1 Vacancy
Job Description
Clinical Research Coordinator III
Bachelors degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience.
The Department of Medicine Administrations is seeking qualified applicants for a Clinical Research Coordinator III position. The incumbent of this position will be an integral member of the central study management team. Responsibilities which include but not limited to recruitment of assigned trials interacting with participants within the assigned trials data collection and management AE/SAE reporting scheduling study required procedures and working with Sponsor and CRO for data entry on case report forms or into a computerized data base & UF OnCore data system. As well as serving as serving to train new coordinators hired by divisions and support department Clinical Trial units as a subject matter expert.
Essential Functions;
Training activities that serve to grow the clinical study infrastructure of smaller units.
Participate in staff recruitment for additional coordinators for division(s)/PIs supported by the central study team
Develop coordinate and training for new coordinators for division(s)/PIs supported by the central study team or directed by supervisor
Serve as project manager for studies transitioning from department coordinator to divisional coordinator(s) when units are ready to stand alone in a division.
Serve as a point of contact/subject matter expert for existing clinical trial teams and division administrators
Establish connection with UF CTSI leadership & COM Clinical Rsch Hub and share with department staff and faculty learning opportunities available through CTSI
Serve as interim clinical research manager for division clinical trials teams when need arises as directed by supervisor
Preparation of potential clinical trials
Assisting PI in site evaluation/qualification process and site initiation visit including completing the feasibility questionnaire as well as collection of any documents requested by Sponsor or CRO
Reviewing study protocol and assisting Regulatory Specialist in obtaining cost of services from UF Health/CTSI/outside vendors
Preparing varies required compliance document/forms needed for IRB submission
Management of multiple clinical trials as a clinical research coordinator
Recruiting and entering eligible candidates into research studies after reviewing the risks and benefits of the study and obtaining informed consent
Following patients through IRB approved protocols and coordinating study required procedures with other departments/units
Collecting documenting and maintaining accurate patient records
Obtaining blood or other body fluids samples per clinical trial protocol
Preparing reports to the Institutional Review Board in a timely manner
Facilitating sponsors/monitors visits
Knowing implementing monitoring and assuring the compliance with University of Florida institutional regulations regarding research
Communicating with research sponsors monitoring agencies and the Institutional Review Board(s) in a timely accurate and effective manner
Other duties as assigned; centered around study management and research administration.
$65000 $76500 Annually
Minimum 2 years clinical specializing in clinical research management
In order to be considered you must upload your resume.
Application must be submitted by 11:55 p.m. (ET) of the posting end date.
Employment Type
Full-Time
