Clinical Research Coordinator - 255338

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

We are seeking an experienced Clinical Research Coordinator (CRC) to join a growing research

site in Asheboro, NC focused on internal medicine and addiction clinical trials. The site is actively conducting multiple high-volume studies with strong enrollment activity, offering an opportunity to work in a dynamic and engaging research environment.

This role is ideal for someone who enjoys a fast-paced setting and is comfortable managing the full lifecycle of clinical trials across several protocols.

Key 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
• Quality assurance and quality control (QA/QC)

Support ongoing patient enrollment and screening efforts across multiple studies

Perform and support clinical procedures, including:

• Injections (or willingness to be trained)

Receive and manage investigational product and devices

Assist with monitoring visits, audits, and sponsor communication

Ensure compliance with GCP, protocols, and site SOPs

Effectively prioritize and manage multiple concurrent studies and tasks

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

Required experience with:

• EKGs

Solid understanding of clinical trial processes across the full study lifecycle

Device trial experience is a plus, but not required

Comfortable with technology and electronic systems

Adaptable, proactive, and open to a hands-on, full-scope CRC role

Ideal Candidate Profile

• Strong multitasking and prioritization skills
• Detail-oriented with a focus on accuracy and compliance
• Comfortable in a busy, evolving research environment
• Willing to take ownership of a broad range of responsibilities