Onsite Clinical Research Nurse Coordinator

M3 USA Corporation; Wilmington (NC); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

401(k), 401(k) matching

Dental insurance

Disability insurance

Employee assistance program

Flexible spending account

Health insurance

Life insurance

Paid time off

Vision insurance

Job summary

M3 Wake Research is seeking a Clinical Research Nurse Coordinator to support trial activities at the Wilmington, NC site. You will work under the Principal Investigator to ensure accurate dispensing and dosing of investigational product while coordinating daily study operations.

You will perform protocol-driven procedures, lead patient education in outpatient settings, and maintain source documents and regulatory binders to keep the study compliant.

Qualifications

• RN or LPN licensed in NC, with current ACLS.
• 1–2 years infusion experience.
• 1–2 years clinical research experience preferred.
• Knowledge of IP handling, sterile compounding, infusion and source documentation in a research setting.

Responsibilities

• Follow protocols, procedures, timelines, and inclusion/exclusion criteria.
• Perform infusions as dictated by the clinical trial protocol.
• Handle, prepare, administer, and track investigational product.
• Lead patient consultations and education under the PI.
• Assist with informed consent amendments and process.
• Record vitals, EKGs, phlebotomy, pulmonary function testing, and sample processing.
• Maintain regulatory binders, source documents, and the Delegation of Authority Log.
• Partner with recruitment to meet enrollment goals.
• Communicate with sponsors, CROs, vendors, and participants.
• Attend PSVs, SIVs, IMVs, COVs, and investigator meetings; travel as needed.
• Report non-compliance or audits to site management.

Skills

Communication

Organization

Attention to detail

Independent work

Teamwork

Computer skills

Education

RN or LPN license in NC

ACLS certification

Job description

M3 Wake Research is seeking a Clinical Research Nurse Coordinator to support trial activities at the Wilmington, NC site. You will work under the Principal Investigator to ensure accurate dispensing and dosing of investigational product while coordinating daily study operations.

You will perform protocol-driven procedures, lead patient education in outpatient settings, and maintain source documents and regulatory binders to keep the study compliant.