Clinical Research Coordinator II
Apply now
Job no: 536733
Work type: Staff Full-Time
Location: Jacksonville Campus
Categories: Allied Health, Office/Administrative/Fiscal Support, Health Care Administration/Support
Department:30010100 - JX-DEAN-ADMINISTRATION
Classification Title: |
Clinical Research Coordinator II
|
Classification Minimum Requirements: |
Bachelor's degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.
|
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: |
$50,000 - $60,000 per year.
|
Required Qualifications: |
Bachelor's degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.
A Valid Driver’s license is required. |
Preferred: |
Master'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.
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 necessitates 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: |
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.
This is a time-limited position.
|
Health Assessment Required: |
Yes |
Advertised: Eastern Daylight Time
Applications close: Eastern Daylight Time
Back to search results Apply nowRefer a friend