Clinical Research Coordinator - Duke Cancer Institute

Clinical Research Coordinator - Duke Cancer Institute

Location:

Durham, NC, US, 27710

Work Arrangement:
Hybrid (On‑Site and Remote mix)

Regular or Temporary:
Regular

Requisition Number: 269499

• Coordinate and manage study operations by implementing recruitment and retention strategies, evaluating enrollment feasibility, maintaining participant engagement, and identifying barriers to participation while proposing and implementing solutions across the study lifecycle.
• Recruit, screen, consent, and support participants by working closely with the Principal Investigator and study team; independently conduct and document consent, schedule and conduct study visits, manage repeated participant outreach and follow‑up, and ensure accurate tracking of participant progress across multiple participation pathways.
• Ensure regulatory compliance and study integrity by maintaining regulatory binders, enrollment logs, and system documentation; recording and promptly reporting adverse events; assisting with Delegation of Authority Logs, COI documentation, Data Safety Monitoring Plans, and Duke Research Data Lifecycle requirements.
• Manage and protect study data by accurately entering data into EDC systems, identifying and resolving data discrepancies, investigating missing or incomplete documentation, and ensuring compliance with institutional policies related to data security, provenance, and confidentiality.
• Serve as a key communication and leadership resource by acting as the primary liaison among sponsors, investigators, and study personnel; escalating issues appropriately; supporting onboarding and training of research staff; sharing research updates; and contributing to continuous improvement of research processes.

• Completion of an Associate’s degree
• Two years of relevant research experience
• Completion of the DOCR North Carolina state‑approved Clinical Research Apprenticeship program may substitute for one year of experience

• Experience with human subjects research
  , including informed consent, confidentiality, and adherence to IRB‑approved protocols
• Strong participant‑facing communication skills
  , including conducting outreach and follow‑up via phone and email using standardized scripts
• Experience managing complex operational tracking workflows
  , including monitoring participant status across multiple study pathways
• Advanced knowledge or experience building and maintaining databases using REDCap or similar data capture systems
• Familiarity with clinical research management systems such as OnCore, eREG, Epic/EMR
  , or other EDC platforms

• Ability to meet and maintain Duke and project‑specific training and certification requirements

Anticipated Pay Range: USD $59,829.00 to USD $99,960.00. Duke University considers factors such as scope and responsibilities of the position; candidate’s work experience, education/training, and key skills; internal peer equity; as well as market and organizational considerations when extending an offer.

Benefits include comprehensive medical and dental care programs, generous retirement benefits, and a wide array of family‑friendly and cultural programs to eligible team members. Learn more at (Use the "Apply for this Job" box below)..

Duke is an Equal Opportunity Employer committed to providing employment opportunity without regard to an individual's age, color, disability, gender, gender expression, gender identity, genetic information, national origin, race, religion, (including pregnancy and pregnancy related conditions), sexual orientation, or military status.

Certain jobs at Duke University and Duke University Health System may include essential job functions that require specific physical and/or mental abilities. Additional information and reasonable accommodation(s) can be requested with Duke Access and Accommodations Services (email: DAAS; phone: ).

Nearest Major Market:
Durham

Nearest Secondary Market:
Raleigh

Read more about Duke’s commitment to affirmative action and nondiscrimination e.edu/eeo.