Senior Clinical Data Specialist – Oncology Trials

Duke Clinical Research Institute; Durham (NC); On-site; USD 32,000 - 48,000; Full time

Job summary

Duke Clinical Research Institute, part of Duke Cancer Institute, is seeking a Senior Clinical Research Specialist to support lymphoma trials. You will manage data coordination, entry, and quality across trials, ensuring regulatory compliance and data integrity.

The role emphasizes data security, collaboration with multidisciplinary teams, and adherence to SOPs while supporting the execution of complex clinical studies in oncology.

Qualifications

• Associate's degree required; 1 year of clinical research experience or related work.
• Experience with data entry in a clinical research or healthcare setting preferred.
• Familiarity with Electronic Data Capture (EDC) systems and clinical trial databases.
• Ability to handle multiple software platforms and maintain data accuracy and integrity.

Responsibilities

• Coordinate study operations and participant activities per protocol and SOPs.
• Maintain subject-level and study-level records; assist with study payments and source documentation.
• Enter study data accurately using EDC systems and CRFs/eCRFs; generate summaries/reports.
• Ensure data quality, security, and compliance by following SOPs and managing data provenance.
• Handle biological specimens and communicate effectively with study teams.

Skills

Data management

Data entry

EDC systems

Attention to detail

SOP adherence

Education

Associate's degree

Tools

Microsoft Office

Internet browsers

Job description

Duke Clinical Research Institute, part of Duke Cancer Institute, is seeking a Senior Clinical Research Specialist to support lymphoma trials. You will manage data coordination, entry, and quality across trials, ensuring regulatory compliance and data integrity.

The role emphasizes data security, collaboration with multidisciplinary teams, and adherence to SOPs while supporting the execution of complex clinical studies in oncology.