Clinical Research Coordinator (CRC) Job Opportunity
Location: Lake Worth, FL Site Name: JEM Research Institute Type: Regular Full-time Employee Schedule: Mondays through Fridays, 8:00am - 5:00pm Location: Onsite in Lake Worth, FL (no capabilities for remote or hybrid work)
Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.
We're seeking a Clinical Research Coordinator (CRC) for our clinical research site located in Lake Worth, FL. The CRC will manage and execute Phase I-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced environment and is eager to make an impact in the clinical research industry.
Benefits:
• Our benefits package for full-time employees includes health insurance (medical, dental, and vision) • Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA) • Paid Time Off (PTO) • A variety of disability, accident, and life insurance options • Many more
What We Offer:
• Competitive pay + annual performance incentives • Medical, dental, and vision insurance • 401(k) plan with company match • Paid time off (PTO) and company holidays • A mission-driven culture focused on advancing medicine and improving patient outcomes
Why Join Us?
You'll be part of a growing, mission-driven organization that values its people. At our core, we're committed to bringing innovative medical treatments to patients faster-while creating an environment where employees thrive. If you're passionate about clinical research and ready to make a difference, we'd love to hear from you.
Responsibilities:
• Coordinate all aspects of assigned clinical trials from site initiation to study close-out • Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards • Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs • Manage subject recruitment, informed consent, and retention strategies • Ensure timely data entry and resolution of EDC queries • Report and follow up on all adverse events, serious adverse events, and deviations • Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders • Prepare for and participate in monitoring visits, audits, and inspections • Maintain regulatory documentation and ensure proper training is completed for all study amendments and systems • Execute study procedures such as phlebotomy, ECGs, and sample processing within scope (as trained) • Attend investigator meetings and provide cross-functional support as needed • Maintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory control
Requirements:
• Education & Experience Requirements: • High school diploma or GED • Minimum of 1 year of experience as a Clinical Research Coordinator • Minimum of 2 years of college within a health-related program • Licensed as a Licensed Practical Nurse (LPN) or higher • Bachelor's degree in a health or scientific-related program
• Skills & Qualifications: • Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures • Proficiency in medical terminology and clinical documentation practices • Strong interpersonal, verbal, and written communication skills • Organized, detail-oriented, and capable of managing multiple priorities • Proficient in Microsoft Office and other clinical research systems
Apply Now:
To become a part of a team that's changing the future of healthcare-one trial at a time, apply now.