Clinical Research Specialist, Senior - Cancer Institute

Clinical Research Specialist, Senior - Duke Cancer Institute

Work Arrangement:
Regular or Temporary:
Regular

Requisition Number: 264413

Location:

Durham, NC, US, 27710

Date:
Jan 17, 2026

Be You.

The Duke Cancer Institute’s Brain Tumor Clinical Research Program is seeking a Clinical Research Assistant to join our dynamic team. In this role, you’ll be at the heart of cutting‑edge clinical research, supporting studies that aim to improve outcomes for patients with brain tumors. You’ll contribute to the daily operations of clinical trials, working closely with participants, clinicians, and researchers.

This is a hands‑on role where you’ll manage participant interactions, collect and process biological specimens, and ensure data integrity. You’ll be part of a collaborative environment that values precision, ethics, and innovation. If you’re detail‑oriented, passionate about research, and eager to grow in the clinical research field, this is a great opportunity to make a meaningful impact.

• One year of relevant experience (Bachelor’s degree may substitute for experience).
• Basic Life Saving (BLS) certification from the American Heart Association or Duke‑approved equivalent.

• Experience in clinical research or a healthcare setting.
• Familiarity with Electronic Data Capture (EDC) systems and Case Report Forms (CRFs/eCRFs).
• Strong written and verbal communication skills.
• Ability to work independently and as part of a team.
• Knowledge of ethical guidelines and regulatory requirements for clinical research.

• Must maintain Duke and project‑specific training and certification requirements.
• Must be able to collect, process, and ship research specimens according to protocol.
• This position is hybrid and performed at Duke University or a designated assignment location.

• Screen and consent participants for minimal risk studies, ensuring proper documentation and ethical compliance.
• Coordinate and schedule study visits, prepare necessary materials, and support participant interviews.
• Collect and manage biological specimens, maintain inventory, and ensure proper handling and shipping procedures.
• Enter and verify clinical data using EDC systems, run reports, and ensure data accuracy and completeness.
• Collaborate and communicate with study personnel to resolve routine issues and support study implementation.
• Participate actively in team meetings, committees, and continuing education opportunities.
• Uphold ethical standards in research, especially when working with vulnerable populations, and ensure participant safety.

At Duke Cancer Institute, you’ll be part of a nationally recognized research organization committed to excellence, innovation, and compassionate care. Our Brain Tumor Clinical Research Program is at the forefront of clinical trials, offering you the chance to contribute to life‑changing discoveries.

You’ll work in a supportive environment that values diversity, inclusion, and professional development. Duke offers a vibrant campus community, access to world‑class resources, and a culture of collaboration and discovery.

Duke University provides an annual base salary range for this position as USD $20.76 to USD $31.44. Duke University considers factors such as (but not limited to) 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.

Your total compensation goes beyond the dollars on your paycheck. Duke provides comprehensive and competitive 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)./

Job Code:  CLINICAL RESEARCH SPECIALIST, SR
Job Level: 09

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, sex (including pregnancy and pregnancy related conditions), sexual orientation…