Dynamic CRC: Fast-Paced Clinical Trials

Medix™; Asheboro (NC); On-site; USD 48,000 - 64,000; Full time

Job summary

Medix™ is seeking an experienced Clinical Research Coordinator to join a fast-paced site in Asheboro, NC. You will oversee end-to-end trial activities across multiple protocols, manage patient recruitment and visits, and ensure QA/QC and compliance with GCP and site SOPs. Strong attention to detail and the ability to multitask are essential.

The role focuses on internal medicine and addiction trials with high enrollment and a hands-on, full-scope CRC approach in a dynamic research environment.

Qualifications

• Minimum 1+ year of Clinical Research Coordinator experience.
• Experience in fast-paced or high-activity clinical research settings preferred.
• Ability to manage multiple studies simultaneously with strong attention to detail.

Responsibilities

• Oversee end-to-end clinical trial activities, including study start-up and regulatory documentation.
• Patient recruitment, screening, and informed consent.
• Study visits and follow-up; data entry and query resolution; QA/QC.

Skills

CRC experience

Regulatory documentation

Data entry

GCP compliance

Tools

Electronic systems

Job description

Medix™ is seeking an experienced Clinical Research Coordinator to join a fast-paced site in Asheboro, NC. You will oversee end-to-end trial activities across multiple protocols, manage patient recruitment and visits, and ensure QA/QC and compliance with GCP and site SOPs. Strong attention to detail and the ability to multitask are essential.

The role focuses on internal medicine and addiction trials with high enrollment and a hands-on, full-scope CRC approach in a dynamic research environment.