Find & Apply For Clinical Research Coordinator Jobs in Melrose, Florida

Position Summary The Research Coordinator (CTI Study Coordinator) is the study's clinical and data anchor at The Melrose Center. Reporting to the Executive Director / Co-Principal Investigator, the Coordinator manages participant eligibility screening, baseline health metrics, cohort oversight, and study documentation for the FL-LIFE beta test, and serves as the site's point of coordination with the Mayo Clinic research team. This is a part-time (approximately 24-32 hours/week), grant-funded position through September 30, 2027, with continuation contingent on funding. Essential Duties and Responsibilities Manage participant screening against IRB-approved inclusion/exclusion criteria (adults 21+, county residency, English-speaking, willing to use adaptive technology; excluding recent behavioral-study participants) and maintain screening logs Support the informed consent process and participant onboarding assessments in coordination with the Mayo research coordinator Collect and document baseline and follow-up health metrics (blood pressure, height, weight, BMI) and maintain accurate, complete study records Provide cohort oversight across the 12-week intervention: attendance, participant status, protocol adherence, and data completeness Plan and manage the clinical screening station at monthly health fairs and recruitment events Operate the safety escalation / red-flag referral pathway, routing clinical concerns to the Melrose clinical team per protocol Enter, verify, and quality-check study data; prepare data for monthly implementation reports (RW-03) and support

RW-01/RW-02/RW-04

deliverables Maintain IRB, HIPAA, and human-subjects compliance, including documentation of training and consent records Contribute community-feasibility observations to the project's workstream meetings as requested Support focus groups, post-intervention surveys, and study closeout activities Minimum Qualifications Undergraduate degree in a related field (public health, health sciences, nursing, social or behavioral sciences, or comparable), with study management experience — coordinating or supervising research study operations, protocols, and participant cohorts Strong organization, documentation, and follow-through; comfort with spreadsheets and data entry systems Completion of human-subjects research training (e.g., CITI) prior to participant contact, or willingness to complete during onboarding Ability to pass a Level 2 background screening; reliable transportation; availability for occasional evening/weekend events (including first-Friday health fairs) Preferred Qualifications Graduate degree in a related field, with experience in translational and implementation science (moving evidence-based interventions into real-world community or clinical practice) Clinical research coordination credential or experience (CCRC or equivalent); familiarity with electronic data capture systems and IRB-regulated studies Clinical training or experience (e.g., LPN, RN, medical assistant) a plus for baseline health metrics collection Community-based or rural health experience; knowledge of the Putnam/Clay County community and its health resources.

Pay:

$32.00 - $36.00 per hour

Benefits:

Employee discount

Work Location:

In person