Senior Clinical Research Specialist: Lymphoma Trials

Duke Careers; Durham (NC); On-site; USD 70,000 - 95,000; Full time

Job summary

Duke Cancer Institute in Durham, NC, seeks a Senior Clinical Research Specialist to support the Lymphoma Clinical Research Team. You will contribute to data coordination and management across the lymphoma portfolio, ensuring accuracy and regulatory compliance throughout the trial lifecycle.

You will work with multidisciplinary teams, use Electronic Data Capture systems, assist with scheduling, documentation, and specimen handling, and help ensure data security and robust study conduct in a

Qualifications

• Associate’s degree required.
• One year of relevant clinical research experience required.
• Experience with data entry in a clinical research or healthcare setting preferred.
• Familiarity with Electronic Data Capture (EDC) systems and trial databases.
• Ability to follow SOPs, study protocols, and regulatory requirements.

Responsibilities

• Coordinate study operations and participant activities by screening, consent, scheduling visits, and preparing materials per protocol.
• Maintain subject- and study-level documentation and assist with study payments and source definition.
• Enter study data using EDC systems and complete CRFs/eCRFs per protocol; run summaries and reports.
• Ensure data quality, accuracy, security, and provenance; report vulnerabilities as needed.
• Handle research specimens and materials per protocol and lab standards.
• Communicate effectively with study teams and support problem resolution.
• Support team collaboration and pursue professional development.

Skills

Data coordination

Detail-oriented

Communication skills

Education

Associate’s degree

Tools

EDC systems

CRF/eCRF data forms

Job description

Duke Cancer Institute in Durham, NC, seeks a Senior Clinical Research Specialist to support the Lymphoma Clinical Research Team. You will contribute to data coordination and management across the lymphoma portfolio, ensuring accuracy and regulatory compliance throughout the trial lifecycle.

You will work with multidisciplinary teams, use Electronic Data Capture systems, assist with scheduling, documentation, and specimen handling, and help ensure data security and robust study conduct in a