Job Description

About the Opportunity

We’re partnering with a highly respected clinical research site in Ocala, FL that is actively expanding their team. This site is known for its excellence in clinical trial execution, particularly in neurology and Alzheimer’s disease research .

We are seeking an experienced Clinical Research Coordinator (CRC) to lead day-to-day operations on Alzheimer’s clinical trials . This is a fully onsite role with direct involvement in advancing care and treatment options for cognitive disorders.

What You’ll Do

• Coordinate all aspects of assigned clinical trials from startup through close-out
• Conduct subject visits, informed consent discussions, and study-related procedures
• Collaborate closely with investigators, site leadership, and other coordinators
• Manage source documentation, EDC entry, and ensure protocol compliance
• Handle regulatory requirements, monitor visits, and audit preparedness
• Participate in patient recruitment and retention strategies, especially for Alzheimer’s trials
• Report adverse events and safety information in compliance with protocols

What We're Looking For

• 1+ years of experience as a Clinical Research Coordinator at a site or similar setting
• Hands-on experience with Alzheimer’s or neurology trials is strongly preferred
• Familiarity with GCP, ICH, and FDA regulatory standards
• Excellent organization, communication, and time management skills
• Detail-oriented with the ability to work independently in a fast-paced environment
• Certification (CCRC) a plus, but not required

Why Apply?

• Direct-hire opportunity with a high-performing research site
• Join a team making a measurable impact in Alzheimer’s research
• Stable environment with strong site infrastructure and leadership
• Competitive compensation and benefits package

This is an immediate opportunity. Qualified candidates will be contacted quickly for next steps.

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