Clinical Research Coordinator: Trials, Data & Patient Care

Cone Health; Greensboro (NC); On-site; USD 55,000 - 75,000; Full time

Job summary

Cone Health in Greensboro, NC seeks a Clinical Research Coordinator to manage day-to-day clinical research activities and data collection under supervision. The role involves coordinating patient visits, maintaining study documentation, and preparing materials for regulatory review.

Responsibilities include screening for eligibility, obtaining consent, data entry, EMR documentation, and assisting with routine clinical tasks under the PI.

Qualifications

• Requires a bachelor’s or associate degree with related experience.
• Experience handling clinical data and keeping logs.
• Certification in Clinical Research preferred.

Responsibilities

• Assess patients for protocol eligibility.
• Explain study purpose and obtain informed consent.
• Collect data from charts, records, interviews, and tests.
• Document in EMR systems when applicable.
• Coordinate multiple clinical trials and visits.
• Support regulatory submissions to IRB and approvals.
• Perform clinical tasks under PI supervision.
• Complete other duties as assigned.

Skills

Data collection

Informed consent

EMR documentation

Trial coordination

Regulatory submissions

Clinical tasks (ECG, PFT, phlebotomy)

Education

Bachelor's Degree

Associate's Degree with 2 yrs experience

Healthcare/Health-related certification (EMT, Pharm Tech, Rad Tech) with 4 yrs experience

Job description

Cone Health in Greensboro, NC seeks a Clinical Research Coordinator to manage day-to-day clinical research activities and data collection under supervision. The role involves coordinating patient visits, maintaining study documentation, and preparing materials for regulatory review.

Responsibilities include screening for eligibility, obtaining consent, data entry, EMR documentation, and assisting with routine clinical tasks under the PI.