Top 24 Clinical research Jobs in Stuart, Fl

Clinical Research Coordinator
Health Haven —Stuart, FL
- $25 - $35 an hour
- Full-time
- Background check
- HIPAA
- Clinic experience
- Paid holidays
- Health insurance
Quick Apply
23h
Patient Engagement Specialist, Clinical Research
Health Haven —Stuart, FL
- $70,000 - $80,000 a year
- Full-time
- Background check
- Marketing
- Public speaking
- Paid holidays
- Disability insurance
Quick Apply
1d
Registered Nurse - Oncology Clinical Research - Full Time
Jupiter Medical Center —Jupiter, FL
- Full-time
- Nursing
- RN License
- Hospital
Medical Assistant
Florida Cancer Specialists & Research Institute —Stuart, FL
- Full-time
- Background check
- Medical office experience
- BLS Certification
- Tuition reimbursement
- 401(k) matching
8d
Speech-Language Pathologist Clinical Fellow (SLP CF) – School-Based
Soliant —Jupiter, FL
- Full-time
- Classroom
- Master's degree
- Organizational skills
- Continuing education credits
- Health insurance
Quick Apply
Medical Coder
Sunstate Medical Specialists —Jupiter, FL
- Full-time
- Mid-level
- Radiology
Quick Apply
Medical Hematologist/Oncologist - Port Saint Lucie/Stuart
Florida Cancer Specialists & Research Institute —Port Saint Lucie, FL
- Full-time
- Background check
- BC/BE
- Inpatient
- Health insurance
- Tuition reimbursement
Ophthalmologist Medical Retina Glaucoma Comprehensive
EAST FLORIDA EYE INSTITUTE —Stuart, FL
- Full-time
- Private practice
- Surgery
- Office
Quick Apply
Speech Language Pathologist- Clinical Fellow
Pediatric Developmental Services —Port Saint Lucie, FL
- $40 - $49 an hour
- Full-time
- School experience
- Master's degree
- Children
- Vision insurance
Quick Apply
Special Agent: Healthcare Services/Medical Background
Federal Bureau of Investigation —United States
- $103,326 - $133,200 a year
- Full-time
- Mid-level
- Bachelor's degree
- Travel
Critical Care Data and Informatics Lead
Medasource —United States
- $65 - $70 an hour
- Contract
- Remote
- SQL
- Critical & Intensive Care
- Senior level
Quick Apply
2h

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Patient Engagement Specialist, Clinical Research
Health Haven —Stuart, FL
Valid Florida driver's license, reliable transportation, and the ability to travel regularly throughout Stuart, Port St. Lucie, and surrounding communities.
$70,000 - $80,000 a year
Quick Apply
1d
Clinical Research Coordinator I/II/III Opportunities – Multiple Locations Nationwide
Headlands Research —Lake Worth, FL
Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc)…
$45,000 - $100,000 a year
Quick Apply

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Certified Research Registered Nurse
Mount Carmel Health System —Columbus, OH
Licensure / Certification: Current license to practice as a Registered Nurse in the State of Ohio. Experience: Minimum of five years of oncology clinical…
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Research Assistant
OhioHealth —Columbus, OH
Manages complex administrative tasks in support of research administration and clinical trials, including but not limited to screening patients, entering/…

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Clinical Research Coordinator

Health Haven
Stuart, FL

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Job Details

Full-time
$25 - $35 an hour
23 hours ago

Benefits

Paid holidays
Health insurance
Dental insurance
Employee assistance program
Vision insurance
Life insurance
Referral program
Paid sick time

Qualifications

Foreign language proficiency
Clinic experience
Pharmaceutical research experience

Full Job Description

Who We Are

At Health Haven and Health Synergy Clinical Research, we are building a modern and integrated model of psychiatric care that combines high-quality outpatient treatment, interventional psychiatry, and industry-sponsored pharmaceutical clinical research.

Our mission is to provide compassionate, evidence-based mental health care while helping advance the future of psychiatric treatment through ethical clinical research and innovative therapeutic approaches. With continued expansion across Florida, our organization offers physicians the opportunity to grow within a collaborative, high-performing environment focused on clinical excellence, innovation, operational efficiency, and long-term professional development.

We are committed to creating an environment where physicians can thrive clinically, professionally, and financially while working alongside an experienced multidisciplinary team dedicated to exceptional patient care.

Who You Are
You are a detail-oriented and highly organized Clinical Research Coordinator with experience managing clinical trials and working directly with patients. You bring a strong understanding of research protocols, regulatory standards, and patient care, along with the ability to balance multiple responsibilities in a fast-paced environment. You are proactive, professional, and collaborative, with a commitment to accuracy, compliance, and delivering a positive participant experience.

What You’ll Do
You will oversee the day-to-day coordination of clinical trials, ensuring protocol adherence, regulatory compliance, and high-quality data collection. You will work closely with investigators, sponsors, and participants to support study execution, patient safety, and overall study success, particularly within obesity and weight loss clinical trials.

Adverse Event Monitoring: Track, document, and report adverse events and protocol deviations in accordance with regulatory requirements
Collaboration & Stakeholder Communication: Coordinate with Principal Investigators, sponsors, monitors, and regulatory bodies to support study progress and resolve inquiries
Data Collection & Management: Accurately collect, document, and enter study data into electronic systems, ensuring completeness and integrity
Patient Recruitment & Screening: Identify, screen, and enroll eligible participants, including obtaining informed consent and reviewing medical records
Regulatory Compliance: Maintain compliance with FDA, GCP, IRB, and HIPAA guidelines, ensuring all study activities meet required standards
Site Preparation & Documentation: Maintain regulatory binders, case report forms, and essential study documents in audit-ready condition
Specimen Handling: Collect, process, store, and ship biological samples in accordance with study protocols when applicable
Study Coordination: Manage daily clinical trial operations, including scheduling subject visits, coordinating procedures, and ensuring protocol adherence
Subject Visit Management: Coordinate participant visits, follow-ups, and study-related procedures to ensure a smooth and compliant experience
Other Duties as Assigned: Support additional clinical research activities and operational needs as required

What You’ll Bring

Bachelor’s degree or higher required
1+ year of clinical research experience required
1+ year of phlebotomy experience preferred
Experience working directly with patients in a clinical setting
Strong understanding of medical terminology
Excellent organizational skills and attention to detail
Ability to work independently with minimal supervision
Strong critical thinking and problem-solving abilities
Professionalism and ability to maintain composure in all situations
Strong interpersonal and communication skills with a positive, team-oriented approach
Spanish language proficiency required

What We Offer

Comprehensive Medical Plans
Dental Insurance
Vision Insurance
Employer-paid Life Insurance
Employee Assistance Program (EAP)
Paid Vacation Time
Paid Sick Time
Paid Federal Holidays
Referral Program
Opportunities for growth and development

Equal Opportunity Employer
We are an equal opportunity employer and comply with all applicable federal, state of Florida, and local employment laws. Employment decisions are made without regard to race, color, religion, sex, pregnancy, national origin, age, disability, genetic information, marital status, veteran status, or any other status protected by law. We are committed to maintaining a workplace free from discrimination, harassment, and retaliation, and to fostering an inclusive environment where all employees are treated with fairness, dignity, and respect.

All positions requiring Florida Care Provider Background Screening through the Clearinghouse are subject to background screening requirements under House Bill 531 (2025). For more information, please visit the Care Provider Background Screening Clearinghouse Education and Awareness website at https://info.flclearinghouse.com

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Refine Your Search

clinical research jobs in stuart, fl

Clinical Research Coordinator

Patient Engagement Specialist, Clinical Research

Registered Nurse - Oncology Clinical Research - Full Time

Medical Assistant

Speech-Language Pathologist Clinical Fellow (SLP CF) – School-Based

Medical Coder

Medical Hematologist/Oncologist - Port Saint Lucie/Stuart

Ophthalmologist Medical Retina Glaucoma Comprehensive

Speech Language Pathologist- Clinical Fellow

Special Agent: Healthcare Services/Medical Background

Critical Care Data and Informatics Lead

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