Job Information
University of Florida Clinical Research Coordinator II in Jacksonville Campus, Florida
Clinical Research Coordinator II
Apply now (https://secure.dc4.pageuppeople.com/apply/674/gateway/default.aspx?c=apply&lJobID=532807&lJobSourceTypeID=796&sLanguage=en-us) Job no: 532807
Work type: Staff Full-Time
Location: Jacksonville Campus
Categories: Allied Health, Health Care Administration/Support
Department: 30010100 - JX-DEAN-ADMINISTRATION
Classification Title:
Clinical Research Coordinator II
Job Description:
Work independently and proactively to coordinate all necessary activities required to set up and
monitor a study, completing accurate study status reports and maintaining study documentation.
Submission of protocol, consent documents for IRB approval and assist in preparing regulatory
submissions as requested
Work at UF research locations prescreening, consenting and enrolling participants in research studies
Conduct study visits and follow ups including functions necessary for successful completion of all
protocol required visits/procedures such as vital signs, phlebotomy, diagnostic tests, dispensing of
investigational product, scheduling, drug accountability/reconciliation and organizational tasks as needed.
Help Investigators with proposal development, progress reports, budget creation, regulatory
paperwork and study files.
Other duties as assigned by CRO/ORA leadership
Expected Salary:
Enter advertised salary here.
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:
Masters 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.
Experience in phlebotomy and clinical research is preferred.
Excellent interpersonal skills and the ability to prioritize and effectively communicate verbally and in writing.
Coordinates multiple tasks and work independently and productively in a fast paced, deadline-oriented
environment.
This position requires proficiency in data management and superior organization skills.
Integrity, careful attention to detail; ability to maintain confidentiality, demonstrate professionalism and
respect for subjects’ rights and individual needs; willing to learn and maintain skills in accordance with
HIPAA regulations and Good Clinical Practice guidelines.
Special Instructions to Applicants:
For example, In order to be considered, you must upload your cover letter and resume.
Application must be submitted by 11:55 p.m. (ET) of the posting end date.
Health Assessment Required:Yes
Advertised: 04 Sep 2024 Eastern Daylight Time
Applications close: 18 Sep 2024 Eastern Daylight Time
