Clinical Research Coordinator II
About The Position
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.
Requirements
- Bachelor's degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.
Nice To Haves
- 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.
- Proficiency in data management and 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.
Responsibilities
- coordinate all necessary activities required to set up and monitor a study
- complete accurate study status reports
- maintain study documentation
- submission of protocol, consent documents for IRB approval
- assist in preparing regulatory submissions as requested
- 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
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
1-10 employees
