Clinical Research Nurse & Study Coordinator (On-site)

bethanymedical; High Point (NC); On-site; USD 65,000 - 95,000; Full time

Benefits offered by this job

Competitive Salary

Medical, Dental & Vision Insurance

Company-Paid Life Insurance

Short-Term & Long-Term Disability

401(k) Retirement Plan

PTO & Holidays

CE Opportunities

Professional Development & Training

Education Certification Support

Job summary

Peters Medical Research is seeking a Registered Nurse/Clinical Research Coordinator to join our on-site clinical research team in North Carolina. The role combines nursing care with study coordination across Phase I–IV trials, ensuring protocol adherence and patient safety.

The ideal candidate has an RN license, strong clinical assessment and communication skills, and the ability to manage multiple studies and visits in a fast-paced environment.

Qualifications

• Current, unrestricted Registered Nurse (RN) license.
• Master’s Degree preferred.
• Bachelor’s Degree required.
• Phlebotomy certification required.
• Current BLS certification.
• Clinical research experience is preferred but not required.
• Current GCP certification is preferred but not required.
• Ability to perform venipuncture and IV placement or willingness to become proficient.
• Strong clinical assessment and patient-care skills.

Responsibilities

• Coordinate and conduct assigned Phase I–IV clinical research studies in accordance with study protocols, GCP, IRB requirements, sponsor requirements, and site policies.
• Conduct screening, enrollment, study visits, follow-up visits, and other protocol-required activities.
• Review medical records and assist in assessing potential research participants against protocol inclusion/exclusion criteria.
• Obtain and document medical histories, medications, vital signs, ECGs, laboratory results, and other clinical information.
• Perform venipuncture, IV placement, blood collection, specimen processing, ECGs, and other protocol-required procedures within training and scope of practice.
• Administer investigational products, infusions, injections, and protocol-required medications when appropriately delegated and permitted.
• Monitor participants during dosing, infusions, and research procedures and promptly identify and escalation adverse events or changes in clinical status.
• Assist Investigators with the assessment, documentation, and follow-up of adverse events and safety events.
• Provide clinical support during medically complex and Phase I research visits, including PK visits and prolonged observation periods.
• Complete accurate and timely source documentation and maintain complete research records.
• Enter study data into EDC and other sponsor systems and resolve data queries within required timelines.
• Assist with maintaining regulatory and essential study documents and required training records.
• Manage laboratory kits, specimens, processing, storage, shipment, and associated documentation according to protocol requirements.
• Assist with investigational product accountability and documentation when delegated.
• Coordinate participant scheduling, laboratory testing, imaging, medical records, and other protocol-required services.
• Communicate professionally with sponsors, CROs, CRAs, vendors, laboratories, IRBs, Investigators, and research participants.
• Assist with site initiation visits, monitoring visits, audits, inspections, and study closeout activities.
• Identify and promptly report protocol deviations, documentation deficiencies, safety concerns, and operational issues.
• Serve as a clinical resource to other Research Coordinators and assist with clinically complex subjects and procedures.
• Support clinical research marketing activities, as needed.
• Maintain all required professional credentials, certifications, and clinical research training.

Skills

Diligence & accuracy

Clinical terminology

Communication skills

Organizational skills

Multitasking

EMR/EDC proficiency

Independent work

Patient interaction

Team collaboration

Education

Bachelor’s Degree

Master’s Degree preferred

Phlebotomy certification

BLS certification

GCP certification preferred

Tools

EMR

EDC

Microsoft Office

Job description

Peters Medical Research is seeking a Registered Nurse/Clinical Research Coordinator to join our on-site clinical research team in North Carolina. The role combines nursing care with study coordination across Phase I–IV trials, ensuring protocol adherence and patient safety.

The ideal candidate has an RN license, strong clinical assessment and communication skills, and the ability to manage multiple studies and visits in a fast-paced environment.