Nurse Coordinator

Key Responsibilities

• Screen candidates for clinical trials by reviewing medical records and ensuring protocol-required testing is completed.
• Collect, enter, and maintain clinical trial data in binders and electronic databases; attend procedures to capture non-standard-of-care data.
• Upload imaging files for review and troubleshoot transmission errors.
• Prepare for and support monitoring visits, ensuring data completeness, accuracy, and audit-readiness.
• Document and report adverse events, including coordinating with outside medical facilities for records.

Qualifications

• Active, unrestricted Registered Nurse (RN) license.
• 2–3 years of clinical research coordination or equivalent clinical trial experience.
• Strong knowledge of FDA regulations, Good Clinical Practice (GCP), and IRB processes.
• Proficiency with electronic data capture systems and medical record documentation.
• Excellent organizational and documentation skills with ability to maintain audit-ready records.
• Strong communication and interpersonal skills for working with investigators, monitors, and clinical staff.

Pay

Not specified

Schedule

~20 hours per week