Clinical Research Coordinator II

University of Florida College of Medicine - Jacksonville; Jacksonville (FL); On-site; USD 55,000 - 65,000; Full time

Job summary

The University of Florida College of Medicine - Jacksonville is seeking a Clinical Research Coordinator II to coordinate and perform research and regulatory tasks across multiple clinical studies. The CRC II screens, consents, conducts visits, and maintains study documentation in accordance with protocols and IRB requirements.

Responsibilities include preparing regulatory submissions, assisting with budget and protocol development, and coordinating activities with investigators and research

Qualifications

• Bachelor's degree in an appropriate area and two years of relevant experience, or an equivalent combination of education and experience.
• Valid driver's license.

Responsibilities

• Coordinate and perform research activities across multiple clinical studies in accordance with protocols.
• Screen and consent patients in clinics and conduct required study visits and procedures.
• Prepare regulatory submissions and maintain study documentation for IRB approval and approvals.
• Assist investigators with proposal development, progress reports, and budget creation.
• Manage study timelines, data collection, drug accountability and regulatory paperwork as needed.

Skills

Clinical research coordination

IRB/regulatory submissions

Phlebotomy

Education

Bachelor's degree in an appropriate area

Job description

Work Type

Staff Full-Time

Location

Jacksonville Campus

Categories

Allied Health, Office/Administrative/Fiscal Support, Grant or Research Administration, 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

The Clinical Research Office (CRO) in the Office of Research Affairs (ORA), Dean’s Administration, College of Medicine-Jacksonville is looking for a Clinical Research Coordinator II to assist coordinating, engaging and performing research and regulatory functions for clinical research studies. The CRC II will screen and consent patients in different clinics and will conduct research visits as required by the research protocols. He/she will perform functions necessary for successful completion of all protocols including but not limited to required visits/procedures such as vital signs, phlebotomy, diagnostic tests, dispensing of investigational product, scheduling, drug accountability/reconciliation and organizational tasks, where appropriate and as delegated by the investigator, in accordance with protocol/sponsor requirements. This position will work on clinical research studies across many different disciplines, interacting with numerous research teams from the inception of a clinical trial though the close out. 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. Conducts 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. Background Check is Required. Hiring is contingent upon eligibility to work in the US. Searches are conducted in accordance with Florida's Sunshine Law Health Assessment Required: Yes.

Expected Salary

$55,000-$65,000 based on education and experience

Required Qualifications

• Bachelor's degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.
• Valid driver's license.

Preferred

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. 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.