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Clinical Research Coordinator

Job in Inverness, Citrus County, Florida, 34453, USA
Listing for: Search Influence
Per diem position
Listed on 2026-02-03
Job specializations:
  • Healthcare
    Clinical Research
  • Research/Development
    Clinical Research
Salary/Wage Range or Industry Benchmark: 20 - 35 USD Hourly USD 20.00 35.00 HOUR
Job Description & How to Apply Below

Overview

Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives. We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. We are actively hiring a Clinical Research Coordinator at our Inverness research site.

The Clinical Research Coordinator (CRC) is responsible for the ethical and accurate coordination and administration of clinical trials under the direction of the Site Manager, the Principal Investigator, and the Medical Director. The CRC will perform diverse administrative and clinical duties requiring analysis, sound judgment, and a high level of knowledge of study-specific protocols, while providing an impeccable patient experience in every interaction.

Shift: Monday-Friday, 7 AM - 4 PM (occasional weekends) |
Location: 411 West Highland Boulevard, Inverness, FL 34452 |
Compensation: Hourly rate based on experience

Benefits: Health, dental, and vision insurance plans, 401(k) with 4% match, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 10 company holidays.

Responsibilities
  • Maintain familiarity with FDA regulations for clinical research
  • Administratively and clinically manage approximately six to ten clinical trials
  • Adhere to company Standard Operating Procedures, Good Clinical Practice and study protocols
  • Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials
  • Obtain Informed Consent from study participants and verify documentation
  • Screen potential study participants for inclusion/exclusion criteria
  • Schedule and conduct study visits per protocol requirements, including but not limited to the following:
    • Dispense study medication in a professional and accountable manner
    • Collect, process, and ship blood/urine specimens
    • Perform ECGs, obtain vital signs
    • Administer questionnaires/diaries
  • Complete source documentation and maintain timely completion of case report forms
  • Ensure prompt reporting of events to sponsor and IRB
  • Assess participant’s condition and report any significant variations from baseline measurements to Principal Investigator
  • Submit timely patient reimbursement requests to financial team for patient’s participation in protocol
  • Ensure the filing and maintenance of all regulatory documents
  • Schedule and prepare for monitoring visits
  • Maintain communication with Principal Investigator, Sub Investigators, Assistants, sponsors, IRB
  • Other duties as assigned by management
Qualifications
  • Bachelor’s degree preferred
  • Associate's degree in nursing or related field preferred
  • Two years in a related healthcare position
  • Pleasant, outgoing, and mature. Good communication and time management skills. Attention to detail. Self-disciplined and motivated. Diligent and persistent.
  • High level of integrity and accountability
  • Ability to function effectively and positively in a team environment
  • Must have the ability to establish and maintain good working rapport with study patients, physicians, investigators, referring physicians, research staff and clinic
  • Must exhibit accurate, complete, legible and timely use of communication methods
  • Familiar with medical terminology
  • BCLS training required
  • Recommended to sit for Certified Clinical Research Coordinator certification after two years’ experience
About Flourish Research

Flourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Flourish Research represents one of the industry’s most progressive and diversified clinical trial companies with robust capabilities in cardiology/metabolic disorders/renal, CNS, pulmonology, and vaccines. Flourish Research is committed to diversity, inclusion, and a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect.

We emphasize education, acceptance, and inclusion to reflect the diversity of our local communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!

Equal Employment Opportunity
:
Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.

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