Registered Nurse/ Clinical Research Coordinator

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

REGISTERED NURSE / CLINICAL RESEARCH COORDINATOR

“Established Clinical Research Company is Seeking a Registered Nurse / Clinical Research Coordinator to Join Our Team!”

Position Summary

Peters Medical Research is seeking an initiative-taking, detail-oriented Registered Nurse / Clinical Research Coordinator (RN/CRC) to join our growing clinical research team.

The RN/CRC will coordinate and conduct clinical research studies while providing nursing expertise and direct clinical support to research participants and the research team. This position combines traditional Clinical Research Coordinator responsibilities with direct patient care, clinical assessments, medication administration, laboratory procedures, and support of medically complex research visits.

The RN/CRC will assist with assigned clinical trials from study startup through closeout and serve as a clinical resource to other research staff. The ideal candidate will possess excellent organizational and communication skills, strong clinical judgment within the nursing scope of practice, and a commitment to patient safety, research quality, and protocol compliance.

Essential Duties & 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.

Requirements

• 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.

Preferred Qualifications

• Clinical research coordination experience.
• Experience with IV infusions and medication administration.
• ACLS certification.
• Familiarity with GCP, FDA regulations, IRB requirements, EDC and IRT systems, and clinical trial documentation.
• Experience in internal medicine, cardiology, gastroenterology, emergency medicine, critical care, infusion therapy, or another medically complex clinical setting.

Skills & Abilities

• Excellent diligence with a strong focus on quality and accuracy.
• Strong knowledge of medical and clinical research terminology.
• Excellent verbal, written, and interpersonal communication skills.
• Strong organizational and time-management abilities.
• Ability to manage multiple studies, participants, deadlines, and competing priorities.
• Proficiency with Microsoft Office, EMR, EDC, and computer-based documentation systems.
• Ability to work independently while functioning effectively as part of a multidisciplinary research team.
• Friendly, professional, and compassionate interaction with patients and research staff.
• Resolute and dependable with the ability to complete assignments and deliverables within required timelines.
• Strong critical thinking skills and willingness to assist other members of the research team.
• Commitment to patient safety, confidentiality, protocol compliance, and research quality.

Schedule & Operational Requirements

• Core clinic hours are 8:00 a.m. to 5:00 p.m., Monday through Friday.
• Some flexibility may be required for early-morning, late-day, weekend, or extended research visits based on study requirements.
• This is not a remote position and requires direct patient care and on-site participation in clinical research activities.
• Must be able to remain on-site for prolonged or time-sensitive research visits when required.
• Must be able to perform venipuncture, IV procedures, collect and process biological specimens, and perform other direct clinical research procedures.

Professional Expectations

The RN/CRC is expected to function as both a clinical research nurse and study coordinator, balancing direct patient care with study coordination responsibilities.

The successful candidate must consistently follow study protocols, site policies, SOPs, sponsor instructions, and established research workflows. All documentation must be accurate, complete, contemporaneous, and maintained within required timelines.

Competitive Benefit Package Includes:

• Competitive Salary
• Medical, Dental & Vision Insurance
• Company-Paid Life Insurance
• Short-Term & Long-Term Disability
• 401(k) Retirement Plan
• Paid Time Off (PTO)
• Paid Holidays
• Continuing Education Opportunities
• Professional Development & Training
• Clinical Research Education and Certification Support
• And more!

Peters Medical Research is affiliated with Bethany Medical:

Bethany Medical is the largest independent established multi-specialty group in Central North Carolina, serving the Triad and surrounding communities for over thirty-nine years. Bethany Medical is open seven days a week, with thirteen convenient locations and sixteen practices in Greensboro, Winston-Salem, High Point, Kernersville, Jamestown, North Wilkesboro, and Mt. Airy, North Carolina. We have grown to provide the facilities, staff, and support to offer urgent care, primary care, diagnostic testing, outpatient ancillary, and specialty care services on-site. Bethany Medical is staffed with board-certified physicians and providers representing sixteen medical specialties. Practice staff members are known for treating each patient with prompt, personalized care and attention. Bethany Medical employs over sixty-five providers and approximately five hundred and fifty employees.

About the Triad:

The Triad area includes Greensboro (third Largest City in NC), Winston-Salem, High Point, and the surrounding area. The Triad is centrally located in NC with a population of over two million. The Triad is one hour from the mountains and three hours from the beach. Charlotte and Raleigh are one and a half hours from the Triad. The Triad offers all the amenities of a larger city without all the traffic. The Piedmont Triad International Airport is conveniently located in Greensboro with convenient nonstop flights to most major cities. Enjoy an outstanding quality of life with no shortage of arts, entertainment, recreation, shopping, and hundreds of restaurants. The Triad is home to eighty-five colleges and universities, including Wake Forest University, High Point University, UNC-Greensboro, NC A&T, Guilford College, Bennett College, and Greensboro College.