Hospital-Based Clinical Research Coordinator

HCA Healthcare, Inc.; Asheville (NC); On-site; USD 60,000 - 75,000; Full time

Benefits offered by this job

Comprehensive benefits

401(k) plan with match

Tuition assistance

Paid time off

Job summary

Mission Health in Asheville is seeking a Clinical Research Coordinator to screen, enroll and monitor study subjects, ensuring protocol compliance and high-quality data collection across trials. You will work with principal investigators, manage source documentation, coordinate adverse event reporting, and support sponsor inspections and audits in a hospital-based research setting.

This role requires a Bachelor's degree if possible and at least one year CRC experience, plus strong communication

Qualifications

• Bachelor's Degree preferred; experience in lieu of education is considered.
• Knowledge of federal regulations, good clinical practices (GCP).
• Knowledge of medical and research terminology.
• Computer skills including use of clinical trial database, electronic data capture, and MS Word or Excel.
• Excellent Verbal and written communication skills; Excellent interpersonal skills.

Responsibilities

• Screen, enroll and follow study subjects per protocol requirements.
• Ensure protocol compliance and close monitoring of subjects.
• Complete study-specific case report forms and source documentation.
• Submit adverse event reports and manage data quality and integrity.
• Generate and track drug/device shipments and supplies as needed.
• Assist sponsor and FDA audit teams and respond to monitoring findings.

Skills

Regulatory knowledge

GCP knowledge

Clinical terminology

Clinical trial database

Electronic data capture

MS Word

MS Excel

Verbal communication

Written communication

Team collaboration

Education

Bachelor's degree preferred

Tools

Clinical trial database

Electronic data capture (EDC)

MS Word

MS Excel

Job description

Mission Health in Asheville is seeking a Clinical Research Coordinator to screen, enroll and monitor study subjects, ensuring protocol compliance and high-quality data collection across trials. You will work with principal investigators, manage source documentation, coordinate adverse event reporting, and support sponsor inspections and audits in a hospital-based research setting.

This role requires a Bachelor's degree if possible and at least one year CRC experience, plus strong communication