Clinical Research Specialist, Senior - Duke Cancer Institute at Duke Careers

Durham, North Carolina, United States -

Full Time

Start Date

Immediate

Expiry Date

30 Jul, 26

Salary

31.44

Posted On

01 May, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical research, Data management, Regulatory documentation, Participant recruitment, Study coordination, Oncology research, Cancer genetics, Chart abstraction, Quality assurance, IRB submissions, Database development, Protocol development, Communication skills, Organizational skills, Data integrity

Industry

IT Services and IT Consulting

Description

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. Be You. The Duke Cancer Institute’s Cancer Control & Population Sciences Clinical Research Program (CCPS) is seeking a Clinical Research Specialist, Sr. to join a collaborative and mission‑driven research team. In this role, you will support a diverse portfolio of cancer research studies—with a primary focus on Duke Clinical Cancer Genetics and contributions to the Supportive Care & Survivorship Center and the Center for Onco‑Primary Care. You will play a hands‑on role in day‑to‑day clinical research operations, supporting minimal‑risk studies through participant recruitment and retention, data collection and management, regulatory documentation, and study coordination activities under the oversight of the Oncology Clinical Research Unit (CRU). Your work will directly support cancer research across multiple disease areas, including pancreatic, prostate, and breast cancer, as well as collaborative genetics studies. This is an excellent opportunity if you enjoy structured work, collaboration with investigators and research teams, and contributing to meaningful research that impacts patient care and survivorship. You will build and apply skills across study operations, data management, ethics, and regulatory compliance, with opportunities for professional development and training. Minimum Requirements Associate’s degree One year of relevant research or clinical experience Completion of the DOCR North Carolina state‑approved Clinical Research Pre‑Apprenticeship program may substitute for one year of required experience Ability to use standard computing software and web‑based applications (e.g., Microsoft Office, internet browsers) Preferred Qualifications Prior oncology and/or clinical research experience Experience or exposure to cancer genetics research Experience with clinical trials coordination and regulatory documentation Familiarity with Epic (including SLICER/DICER), REDCap, Progeny, and iRIS Experience with data entry, database development, and research project coordination Other Requirements Ability to follow established protocols, SOPs, and institutional policies Strong organizational, communication, and documentation skills Comfort working with participant data while maintaining confidentiality and data integrity Be Bold. Support clinical research operations and study management by maintaining participant‑ and study‑level documentation, preparing materials for study visits, assisting with monitoring and audits, and supporting study close‑out activities under supervision. Recruit, consent, and support research participants for minimal‑risk studies in accordance with IRB‑approved protocols, including survey studies, registries, repositories, and observational research. Collect, enter, and manage research data by developing and maintaining data collection tools, performing chart abstraction, correcting data discrepancies, ensuring quality assurance, and following all data security and provenance requirements. Assist with regulatory and ethical oversight by preparing IRB submissions, maintaining compliance documentation, supporting adverse event reporting for minimal‑risk studies, and following sponsor and institutional reporting requirements. Collaborate with investigators and study teams by participating in study meetings, contributing to progress reports, assisting with protocol development for simple studies, and helping prepare funding proposal materials. Demonstrate leadership and professional growth by completing required training, applying learned skills, assisting with peer training, and navigating Duke research processes with adaptability and strong interpersonal skills. Choose Duke. At Duke University, you’ll be part of a world‑class institution committed to excellence, discovery, and inclusion. The Duke Cancer Institute brings together clinicians, researchers, and staff who are united by a shared mission: improving outcomes for patients through innovative, patient‑centered research. Within CCPS, you’ll work on multi‑institutional and investigator‑initiated studies that influence cancer prevention, survivorship, and genetics research—work that truly matters. Duke offers a collaborative research environment, access to cutting‑edge tools and systems, and opportunities for continuous learning and career development. Job Code: 00000803 CLINICAL RESEARCH SPECIALIST, SR Job Level: 09 Anticipated Pay Range: 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: https://hr.duke.edu/benefits/ Equal Opportunity Employer: 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. Duke aspires to create a community built on collaboration, innovation, creativity, and belonging. Our collective success depends on the robust exchange of ideas—an exchange that is best when the rich diversity of our perspectives, backgrounds, and experiences flourishes. To achieve this exchange, it is essential that all members of the community feel secure and welcome, that the contributions of all individuals are respected, and that all voices are heard. All members of our community have a responsibility to uphold these values. Essential Physical Job Functions: 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@duke.edu; phone: 919-668-1267).

Responsibilities

The specialist will support clinical research operations by managing participant documentation, data collection, and regulatory compliance for cancer studies. They will also collaborate with investigators to facilitate participant recruitment, study visits, and the preparation of research materials.