Clinical Research Coordinator

What you’ll do

Clinical Research & Study Management

• 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.

Patient Care & Clinical Responsibilities

• Provide clinical assessment and care to adult study participants within your scope of practice and study requirements.

• Perform and/or oversee procedures including:

• Blood draws/phlebotomy

• ECGs

• Pulmonary function testing

• Vital signs

• 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.

Data & Documentation

• 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.

Qualifications

• Current RN or NP license with the ability to practice with an adult patient population.

• Bachelor’s degree in nursing required; Master’s degree for NP candidates.

• Previous direct patient care experience required.

• Clinical research experience is highly preferred.

• 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 daily.

Why join monroe biomedical research?

• Join a growing clinical research organization.

• Combine patient care with innovative clinical research.

• Contribute directly to medical advancements and emerging treatments.

• Work with a collaborative, mission-driven team.

• Gain experience across a variety of clinical studies.

• Build opportunities for professional growth and leadership.