Oncology Clinical Research Data Specialist

Trinity Health; Hartford (CT); On-site; USD 50,000 - 65,000; Full time

Benefits offered by this job

Great benefits from Day 1

Job summary

Trinity Health Of New England is seeking a detail-oriented Clinical Research Data Assistant to support its Oncology Clinical Research Program. You will collect, manage, analyze, and report clinical data to ensure compliance with study protocols and sponsor expectations.

The role requires EPIC experience, familiarity with research databases, and the ability to collaborate with coordinators, investigators, and sponsors to maintain data integrity across trials.

Qualifications

• Bachelor's degree preferred; equivalent combination of education and relevant experience will be considered.
• Experience in a clinical healthcare setting with oncology terminology and electronic medical records is required.
• Experience navigating EPIC is required; experience with research databases such as Medidata Rave, REDCap, and EPIC SlicerDicer preferred.

Responsibilities

• Collect, review, and enter study data from medical records, laboratory reports, source documents into protocol databases.
• Ensure timely completion of CRFs and resolution of data queries within sponsor timelines.
• Evaluate source documentation for accuracy, completeness, and protocol compliance.
• Maintain study databases and monitor participant follow-up activities for ongoing trials.
• Utilize multiple data platforms including EHRs and research systems to identify, track, and analyze data.
• Assist with tracking, processing, and shipment of biological specimens as required.

Skills

Data entry

Data integrity

Analytical skills

Education

Bachelor's degree

Tools

EPIC

Medidata Rave

REDCap

EPIC SlicerDicer

Job description

Trinity Health Of New England is seeking a detail-oriented Clinical Research Data Assistant to support its Oncology Clinical Research Program. You will collect, manage, analyze, and report clinical data to ensure compliance with study protocols and sponsor expectations.

The role requires EPIC experience, familiarity with research databases, and the ability to collaborate with coordinators, investigators, and sponsors to maintain data integrity across trials.