Clinical Research Coordinator

Who We Are
At Health Synergy Clinical Research and Health Haven, we are united by a mission to prioritize patient safety and advance innovative mental health care. We support individuals seeking clarity, hope, and better outcomes through ethical, patient-centered research and treatment. Our in-person clinics across Florida provide expert psychiatric and mental wellness 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

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