Clinical Research Coordinator: Study Ambassador & Compliance Lead

SupportFinity™; Lexington (KY); On-site; USD 50,000 - 70,000; Full time

Job summary

SupportFinity™ is seeking a Clinical Research Coordinator in Lexington, KY, to manage clinical research tasks critical to study compliance and participant monitoring. Responsibilities include coordinating clinical trials, managing adverse event documentation, and communicating effectively with sponsors.

The ideal candidate should have at least 1 year of clinical research experience, formal medical training, and strong organizational skills. The position may include flexible hours, including weekends and overtime.

Qualifications

• 1 year of experience in clinical research.
• Ability to perform clinical, laboratory, and diagnostic tests.
• Exceptional listening, written, and verbal communication skills.

Responsibilities

• Manage and document Adverse Event reporting.
• Coordinate clinical trials per FDA requirements.
• Ensure compliance with federal regulations.

Skills

Clinical research experience

Medical terminology

Independent work

Multi-tasking

Communication skills

Organizational skills

Education

Completion of formal medical training or healthcare experience

Job description

SupportFinity™ is seeking a Clinical Research Coordinator in Lexington, KY, to manage clinical research tasks critical to study compliance and participant monitoring. Responsibilities include coordinating clinical trials, managing adverse event documentation, and communicating effectively with sponsors.

The ideal candidate should have at least 1 year of clinical research experience, formal medical training, and strong organizational skills. The position may include flexible hours, including weekends and overtime.