Clinical Research Nurse Coordinator: Trial Operations Lead

M3USA; Wilmington (NC); On-site; USD 70,000 - 95,000; Full time

Benefits offered by this job

401(k) with match

Health insurance

Disability insurance

Flexible spending account

Life insurance

Paid time off

Vision insurance

Employee assistance program

Job summary

M3 Wake Research is hiring a Clinical Research Nurse Coordinator for our Wilmington, NC on-site team. You will support the PI by performing trial-related procedures, dispensing and dosing investigational product, and coordinating daily study activities with site staff and sponsors.

The position requires NC RN or LPN licensure, ACLS, and 1–2 years of infusion experience, with a preference for prior clinical research involvement. Travel to meetings may be involved.

Qualifications

• Registered nurse or licensed practical nurse in NC.
• Current ACLS provider card.
• 1–2 years of infusion experience.
• Ideally 1–2 years of clinical research experience.
• Solid understanding of FDA regulations, ICH-GCP, and ISO standards.
• Strong communication, organization, and attention to detail.

Responsibilities

• Follow assigned protocols, study procedures, timelines, and criteria.
• Perform infusions as dictated by the protocol.
• Handle, prepare, administer, and track investigational product with inventory accountability.
• Lead patient consultations and education under PI direction.
• Contribute to informed consent processes and amended consents.
• Perform delegated procedures (vitals, phlebotomy, EKGs, etc.) and document in source.

Skills

RN license NC

ACLS

Infusions

Clinical research exp.

Job description

M3 Wake Research is hiring a Clinical Research Nurse Coordinator for our Wilmington, NC on-site team. You will support the PI by performing trial-related procedures, dispensing and dosing investigational product, and coordinating daily study activities with site staff and sponsors.

The position requires NC RN or LPN licensure, ACLS, and 1–2 years of infusion experience, with a preference for prior clinical research involvement. Travel to meetings may be involved.