Top 9 Clinical research associate Jobs in Wildwood, Fl

Clinical Research Coordinator
Citrus Cardiology Consultants, PLLC —The Villages, FL
- $30 - $36 an hour
- Nursing
- RN License
- Ability to walk for extended periods
- Paid holidays
- Health insurance
Quick Apply
12d
Clinical Research Coordinator
Cardiovascular Associates of America —The Villages, FL
- Full-time
- Mid-level
- Office
- Bachelor's degree
Quick Apply
8d
Clinical Research Coordinator
Flourish Research —Leesburg, FL
- $31 - $36 a year
- Full-time
- Vital signs
- HIPAA
- Mid-level
- Paid holidays
- Disability insurance
Quick Apply
Patient Recruitment Associate
Charter Research LLC —The Villages, FL
- Full-time
- Sales
- Clinic
- Associate's degree
Quick Apply
Research Assistant
Flourish Research —Inverness, FL
- Full-time
- Vital signs
- Computer literacy
- Bachelor's degree
- Paid holidays
- Disability insurance
Quick Apply
1d
Patient Recruitment Manager
Renstar Medical Research —Ocala, FL
- Microsoft Outlook
- OSHA
- Mid-level
Quick Apply

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Clinical Research Coordinator

Citrus Cardiology Consultants, PLLC -
The Villages, FL

Quick Apply

Job Details

$30 - $36 an hour
12 days ago

Benefits

Paid holidays
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
Opportunities for advancement

Qualifications

Research ethical considerations
Patient management software
Research project coordination
Clinical information systems
Productivity software
Clinical quality assurance standards
FDA regulations

Full Job Description

Position Summary

Citrus Cardiology Consultants, PLLC is seeking a highly organized and detail-oriented Research Coordinator to support and manage clinical research studies within our growing cardiology practice. The Research Coordinator will work closely with physicians, research sponsors, patients, and regulatory agencies to ensure the successful execution of clinical trials and observational studies focused on cardiovascular health.

The ideal candidate will have experience in clinical research, excellent communication skills, and a passion for advancing cardiovascular medicine through innovative research.

Key Responsibilities

Coordinate all aspects of assigned clinical research studies from startup through closeout.
Screen, recruit, and enroll eligible patients into clinical trials.
Obtain and document informed consent in accordance with study protocols and regulatory guidelines.
Schedule and conduct study visits, assessments, and follow-up appointments.
Collect, review, and accurately enter study data into electronic data capture systems.
Maintain source documents, regulatory binders, and study files.
Ensure compliance with FDA regulations, ICH-GCP guidelines, HIPAA requirements, and institutional policies.
Serve as the primary liaison between investigators, sponsors, contract research organizations (CROs), and study participants.
Coordinate laboratory testing, diagnostic procedures, and cardiovascular assessments as required by study protocols.
Monitor study progress and report adverse events, protocol deviations, and safety concerns in a timely manner.
Prepare for sponsor monitoring visits, audits, and regulatory inspections.
Assist with budgeting, study feasibility assessments, and participant retention strategies.
Support principal investigators in meeting enrollment and study milestones.

Qualifications

Required

Bachelor's degree in Life Sciences, Nursing, Public Health, or a related field; equivalent clinical research experience may be considered.
Minimum of 2 years of clinical research experience.
Knowledge of Good Clinical Practice (GCP), FDA regulations, and human subject protection requirements.
Proficiency with EMR systems and Microsoft Office applications.
Excellent organizational, analytical, and problem-solving skills.
Strong verbal and written communication abilities.
Ability to manage multiple studies simultaneously while maintaining attention to detail.

Preferred

Experience coordinating cardiology or cardiovascular clinical trials.
Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification.
Clinical experience as a Registered Nurse, Medical Assistant, or allied health professional.
Experience with electronic data capture systems and clinical trial management software.

Physical Requirements

Ability to sit, stand, and walk for extended periods.
Ability to assist with patient visits and perform study-related assessments as needed.
Ability to lift up to 25 pounds occasionally.

Benefits

Competitive salary
Health, dental, and vision insurance
401(k) Participation
Paid time off and holidays
Opportunities for professional growth and advancement
Collaborative and patient-focused work environment

Why Join Our Team?

At Citrus Cardiology Consultants, PLLC we are committed to improving cardiovascular outcomes through excellence in patient care and innovative clinical research. Joining our team offers the opportunity to work alongside leading cardiologists while contributing to groundbreaking studies that shape the future of heart health.

Quick Apply

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clinical research associate jobs in wildwood, fl

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator

Patient Recruitment Associate

Research Assistant

Patient Recruitment Manager

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