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Clinical Research Coord II

 
  • University of Florida
  • United States
  • Mar 15, 2023
Full Time - Continuing
About University of Florida
At the University of Florida, we are a people of purpose. We're committed to challenging convention and ourselves. We see things not as they are, but as they could be. And we strive for a greater impact: one measured in people helped...

Job Description:

Classification Title:

Clinical Research Coord 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. Assist with regulatory documents and related start up activities. 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.
Serve as liaison for study participant, investigator, IRB, sponsor and all the healthcare providers contributing to research studies.
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
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:

Please provide letter of intent and Curriculum Vitae.

This is a time-limited position.

This requisition has been reposted. Previous applicants are still under consideration and need not apply.

Applications must be submitted by 11:55 p.m. of the posting end date.
Health Assessment Required: Yes



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    • col-narrow-left   

    Job ID:

    22708

    Location:

    Jacksonville Campus,Duval 
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    Job Views:

    10

    Employment Type:

    Full Time - Continuing
    col-wide   

    Job Description:

    "\n\n\n\n\n\n\n\n\n
    Classification Title:<\/th>\n\n

    Clinical Research Coord II<\/p>\n<\/td>\n<\/tr>\n

    Job Description:<\/th>\n\n
    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. Assist with regulatory documents and related start up activities. Submission of protocol, consent documents for IRB approval and assist in preparing regulatory submissions as requested.<\/div>\n
    <\/div>\n
    Work at UF research locations prescreening, consenting and enrolling participants in research studies.<\/div>\n
    <\/div>\n
    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.<\/div>\n
    <\/div>\n
    Serve as liaison for study participant, investigator, IRB, sponsor and all the healthcare providers contributing to research studies.<\/div>\n
    <\/div>\n
    Help Investigators with proposal development, progress reports, budget creation, regulatory paperwork and study files.<\/div>\n
    <\/div>\n
    Other duties as assigned by CRO\/ORA leadership<\/div>\n<\/td>\n<\/tr>\n
    Expected Salary:<\/th>\n\n

    $50,000-$60,000<\/p>\n<\/td>\n<\/tr>\n

    Minimum Requirements:<\/th>\n\n

    Bachelor\u2019s degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.<\/p>\n<\/td>\n<\/tr>\n

    Preferred Qualifications:<\/th>\n\n

    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.<\/p>\n

    Experience in phlebotomy and clinical research is preferred.<\/p>\n

    Excellent interpersonal skills and the ability to prioritize and effectively communicate verbally and in writing.<\/p>\n

    Coordinates multiple tasks and work independently and productively in a fast paced, deadline-oriented environment.<\/p>\n

    This position requires proficiency in data management and superior organization skills.<\/p>\n

    Integrity, careful attention to detail; ability to maintain confidentiality, demonstrate professionalism and respect for subjects\u2019 rights and individual needs; willing to learn and maintain skills in accordance with HIPAA regulations and Good Clinical Practice guidelines.<\/p>\n<\/td>\n<\/tr>\n

    Special Instructions to Applicants:<\/th>\n\n

    Please provide letter of intent and Curriculum Vitae.<\/p>\n

    This is a time-limited position.<\/p>\n

    This requisition has been reposted. Previous applicants are still under consideration and need not apply.<\/p>\n

    Applications must be submitted by 11:55 p.m. of the posting end date.<\/p>\n<\/td>\n<\/tr>\n

    Health Assessment Required:<\/th>\nYes<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

    <\/p>"

    Posted:

    15/03/2023