Oncology Research Data Specialist – Impactful Trials

Association of Community Cancer Centers; Rockville (MD); On-site; USD 52,000 - 76,000; Full time

Job summary

Trinity Health Of New England seeks a detail-oriented Clinical Research Data Assistant to support our Oncology Clinical Research Program. You will responsibly collect, manage, analyze, and report data to ensure protocol compliance and sponsor expectations.

Collaborating with Coordinators, investigators, providers, and sponsors, you will maintain data integrity across oncology trials, balancing multiple studies and deadlines in a mission-driven health system.

Qualifications

• Bachelor's degree preferred; equivalent experience considered.
• Experience in a clinical healthcare setting with oncology terminology and EMR required.
• Clinical research, coordination, or data management experience preferred.
• EPIC navigation required; familiarity with Medidata Rave, REDCap, and SlicerDicer preferred.

Responsibilities

• Collect, review, and enter study data from sources into databases.
• Ensure timely completion of case report forms and data queries.
• Evaluate source documents for accuracy and protocol compliance.
• Maintain study databases and monitor follow-up activities.
• Use multiple data platforms to identify and analyze participant data.
• Support IRB policies and procedures implementation.
• Collaborate with coordinators, investigators, and providers to verify data.
• Assist with tracking and shipment of biological specimens as required.

Skills

Oncology terminology

EMR systems

EPIC navigation

Data management

Clinical research experience

Education

Bachelor's degree or equivalent

Tools

Medidata Rave

REDCap

EPIC SlicerDicer

EPIC

Job description

Trinity Health Of New England seeks a detail-oriented Clinical Research Data Assistant to support our Oncology Clinical Research Program. You will responsibly collect, manage, analyze, and report data to ensure protocol compliance and sponsor expectations.

Collaborating with Coordinators, investigators, providers, and sponsors, you will maintain data integrity across oncology trials, balancing multiple studies and deadlines in a mission-driven health system.