Clinical Research Coordinator: Study Ops & Patient Impact

CLINICAL TRIALS CENTER OF MIDDLE T; Franklin (TN); On-site; USD 48,000 - 72,000; Full time

Benefits offered by this job

401(k) matching

Dental insurance

Health insurance

Life insurance

Paid time off

Vision insurance

Job summary

The Clinical Trials Center of Middle Tennessee, LLC seeks a motivated Clinical Research Coordinator (CRC) to support the Principal Investigator in daily trial activities, ensure protocol compliance, and coordinate data collection, scheduling, and regulatory documentation.

You will work with the research team, sponsor, and participants, managing source documents, adverse events, and study timelines while maintaining patient safety and IRB requirements.

Qualifications

• Bachelor's degree preferred.
• Clinical Research Coordinator experience: 2 years required.
• Skilled in phlebotomy (venipuncture).
• Excellent verbal and written communication skills.

Responsibilities

• Ensure patient protection and well-being; coordinate daily trial activities.
• Coordinate with the PI to ensure compliance with regulations and sponsor policies.
• Maintain effective communication with sponsor, participants, and study staff.
• Manage study documents, source data, CRFs, and audit readiness.
• Assist in recruitment strategies and informed consent process.

Skills

Verbal and written communication

Phlebotomy

Education

Bachelor's degree (Preferred)

Job description

The Clinical Trials Center of Middle Tennessee, LLC seeks a motivated Clinical Research Coordinator (CRC) to support the Principal Investigator in daily trial activities, ensure protocol compliance, and coordinate data collection, scheduling, and regulatory documentation.

You will work with the research team, sponsor, and participants, managing source documents, adverse events, and study timelines while maintaining patient safety and IRB requirements.