Clinical Research Coordinator: Drive Trials & Data Quality

Piedmont HealthCare, PA; Statesville (NC); Hybrid; USD 52,000 - 57,000; Full time

Benefits offered by this job

Health Insurance

Dental Insurance

Disability Insurance

Life Insurance

Paid Time Off

Vision Insurance

Job summary

Piedmont HealthCare, PA in Statesville, NC is seeking a Clinical Research Coordinator to manage data collection, regulatory documents, and patient records for ongoing studies.

The CRC will recruit and screen participants, assist with consent, perform study procedures, monitor safety, and ensure compliance with GCP/ICH and FDA guidelines while coordinating with investigators and clinic staff.

Qualifications

• Bachelor's degree in a related field.
• 1–2 years of clinical research experience.
• Experience in a clinical environment or medical setting.
• Proficient with Microsoft Office and medical terminology.

Responsibilities

• Collect, record, and maintain study data per protocols.
• Submit regulatory/ethics documents for FDA and others.
• Recruit and screen participants for trials.
• Assist in consent process and patient orientation.
• Maintain source documentation as required.
• Schedule visits and perform study procedures.
• Monitor safety and report adverse events.
• Coordinate with the team and attend huddles.

Skills

Microsoft Office

Medical terminology

Clinical trials

GCP/ICH

Regulatory knowledge

Communication skills

Education

Bachelor's degree

Job description

Piedmont HealthCare, PA in Statesville, NC is seeking a Clinical Research Coordinator to manage data collection, regulatory documents, and patient records for ongoing studies.

The CRC will recruit and screen participants, assist with consent, perform study procedures, monitor safety, and ensure compliance with GCP/ICH and FDA guidelines while coordinating with investigators and clinic staff.