Clinical Research Coordinator

Monroe+Biomedical+Research • Monroe, NC

4d • Onsite

About The Position

Monroe Biomedical Research is seeking an experienced, patient-focused Clinical Research Coordinator to work onsite at its Monroe, North Carolina location. The role combines direct patient care with clinical research coordination, supporting participants throughout the clinical trial process, from screening and study visits through procedures, documentation, and follow-up. The employer particularly prefers candidates with an RN or NP license.

The coordinator manages study visits and activities, follows clinical trial protocols and regulatory requirements, provides clinical assessment and care to adult participants within their scope of practice, and performs or oversees protocol-required procedures. The role also involves participant education, recognizing and communicating adverse events or significant findings, maintaining accurate study documentation and data, coordinating laboratory specimens, and responding to data queries.

This opportunity is intended for an RN or NP who enjoys patient care, works effectively in a fast-paced environment, and wants to contribute to research that advances medicine and expands treatment options. The position requires daily commuting to Monroe, NC.

Requirements

• Current RN or NP license with the ability to practice with an adult patient population.
• Bachelor’s degree in nursing required; Master’s degree required for NP candidates.
• Previous direct patient care experience.
• Strong clinical judgment and commitment to patient safety.
• Excellent organization, documentation, and attention to detail.
• Ability to interpret and follow detailed clinical trial protocols.
• Ability to manage multiple priorities in a fast-paced environment.
• Strong communication and interpersonal skills.
• Professional, compassionate, and patient-focused approach.
• Must commute daily to Monroe, NC.

Nice To Haves

• Clinical research experience is highly preferred.
• RN or NP candidates are preferred.

Responsibilities

• Coordinate clinical trial visits from screening through completion.
• Review protocols and ensure study procedures are completed accurately and on schedule.
• Maintain complete and accurate source documentation.
• Support participant screening, enrollment, and ongoing study activities.
• Collaborate with investigators, sponsors, monitors, and research staff.
• Ensure compliance with GCP, FDA regulations, sponsor requirements, and internal procedures.
• Provide clinical assessment and care to adult study participants within scope of practice and study requirements.
• Perform and/or oversee blood draws or phlebotomy, ECGs, pulmonary function testing, vital signs, and other protocol-required assessments.
• Review medical history, medications, laboratory results, and other clinical information.
• Educate participants on study procedures, medications, and follow-up.
• Recognize and communicate adverse events or clinically significant findings.
• Deliver a professional, compassionate, and patient-centered experience.
• Document study visits, clinical findings, and patient information accurately.
• Enter and maintain study data within sponsor systems and required timelines.
• Process and coordinate laboratory specimens according to protocol.
• Respond to data queries and maintain accurate, inspection-ready records.

Benefits

• Professional growth and leadership opportunities

What This Job Offers

• Job Type: Full-time