Clinical Study Coordinator Jobs in Raleigh, NC (NOW HIRING)

School of Medicine:

Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe. Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more than 6,200 staff, the Duke University School of Medicine along with the Duke University School of Nursing, and Duke University Health System comprise Duke Health, a world-class academic medical center. The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Health Integrated Practice, Duke Primary Care, Duke Home Care and Hospice, Duke Health and Wellness, and multiple affiliations.

The Oncology Clinical Research Unit (CRU) at Duke Cancer Institute's Wake Clinical Research Program is seeking a Clinical Research Coordinator to join our team. In this role, you will help bring innovative cancer treatments and therapies to patients by coordinating complex oncology clinical trials from study startup through closeout.

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This is an exciting opportunity for a research professional who enjoys working directly with patients, investigators, sponsors, and multidisciplinary healthcare teams while contributing to groundbreaking oncology research. You will play a key role in participant recruitment, study coordination, regulatory compliance, data quality, and overall study success.

• Associate's degree.
• Minimum of two years of relevant clinical research experience.
• Completion of the DOCR North Carolina State Approved Clinical Research Apprenticeship Program may substitute for one year of required experience.
• Proficiency using Microsoft Office applications, web-based systems, and other research-related software applications.
• Ability to manage multiple studies and priorities simultaneously while maintaining attention to detail.
• Strong organizational, communication, and problem-solving skills.
• Ability to work collaboratively with investigators, sponsors, research staff, and participants.

• Oncology clinical research experience.
• Clinical trials coordination experience.
• Research-related education, training, or certification.
• Experience working with investigational products and complex clinical trials.
• Experience with participant recruitment, informed consent, and regulatory compliance activities.
• Familiarity with Electronic Data Capture (EDC) systems and clinical research documentation requirements.

• Basic Life Support (BLS) certification from the American Heart Association or Duke-approved equivalent course is required.
• Must maintain Duke and protocol-specific training and certification requirements.
• Ability to work effectively in a fast-paced clinical research environment.
• Position may require interaction with patients, healthcare providers, sponsors, monitors, and regulatory personnel.

This position is onsite. The work is performed on-site at locations in Wake County.

As a Clinical Research Coordinator, you will:

• Recruit, screen, consent, enroll, schedule, and follow study participants in accordance with study protocols and regulatory requirements.
• Conduct and document participant visits, ensuring protocol adherence and participant safety.
• Collaborate closely with Principal Investigators, sponsors, and study teams to successfully conduct clinical research studies.
• Assist with site initiation, monitoring, and closeout activities.

• Maintain study documentation, regulatory binders, enrollment records, and required research files.
• Monitor protocol compliance and ensure adherence to institutional policies, federal regulations, and Good Clinical Practice guidelines.
• Document and report adverse events and protocol deviations in a timely manner.
• Support development of Conflict of Interest (COI), Data Safety Monitoring Plans (DSMPs), and Research Data Security Plans (RDSPs).

• Implement recruitment and retention strategies to support study enrollment goals.
• Evaluate recruitment challenges and recommend solutions to improve participant engagement and retention.
• Assist participants with study-related needs and provide education regarding research participation.

• Enter, review, and maintain accurate study data in Electronic Data Capture systems.
• Identify and resolve data discrepancies and documentation issues.
• Support study budget management, financial milestone tracking, participant reimbursements, and study closeout activities.
• Coordinate with financial teams to ensure timely processing of study-related expenses.

• Serve as a primary liaison between sponsors, investigators, research staff, and study participants.
• Participate in team meetings, committees, task forces, and departmental initiatives.
• Mentor colleagues and serve as a resource for research best practices.
• Pursue ongoing professional development and contribute to scientific presentations and publications when appropriate.

The Wake Clinical Research Program is part of the nationally recognized Duke Cancer Institute, where innovative research, exceptional patient care, and scientific discovery come together to improve the lives of people affected by cancer. As a member of the Oncology Clinical Research Unit, you will contribute to clinical trials that advance cancer treatment and expand access to cutting-edge therapies for patients.

At Duke, you'll work alongside talented physicians, researchers, and healthcare professionals who are committed to excellence, collaboration, and innovation. You'll have opportunities for professional growth, continuing education, and meaningful contributions to research that impacts patient care locally and globally.