Clinical Research Coordinator II

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

Job summary

The University of Florida in Jacksonville seeks a Clinical Research Coordinator II to support coordinating, engaging and performing research and regulatory tasks across multi-disciplinary clinical studies.

You will screen and consent patients, conduct visits, handle vital signs, phlebotomy, diagnostic tests, dispensing investigational products, and regulatory submissions, while maintaining documentation and study status throughout the trial lifecycle.

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.
• Background Check is Required.

Responsibilities

• Coordinate and manage clinical research studies across multiple disciplines.
• Screen and consent patients in clinics and conduct research visits per protocol.
• Prepare regulatory submissions and assist with IRB submissions as requested.
• Maintain study documentation, reports, and drug accountability; ensure protocol adherence.

Skills

Interpersonal skills

Communication

Data management

Attention to detail

Education

Bachelor's degree in an appropriate area

Job description

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 through 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. 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.

Expected Salary

$55,000-$65,000

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.
• Background Check 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.
• 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.

Health Assessment Required

Yes