Oncology Clinical Research Data Specialist

Trinity Health Of New England; Hartford (CT); On-site; USD 52,000 - 70,000; Full time

Benefits offered by this job

Full-time 40h

Benefits from Day 1

Patient-centric environment

Career growth

Job summary

Trinity Health Of New England is seeking a detail-oriented Clinical Research Data Assistant to support our Oncology Clinical Research Program. This role focuses on accurate collection, management, analysis, and reporting of clinical research data to ensure compliance with protocols, regulatory requirements, and sponsor expectations.

The role requires collaboration with Clinical Research Coordinators, investigators, healthcare providers, and sponsors to maintain data integrity across oncology

Qualifications

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

Responsibilities

• Collect, review, and enter study data from medical records and labs into databases.
• Ensure timely CRF completion and resolution of data queries within timelines.
• Evaluate source documentation for accuracy and protocol compliance.
• Maintain study databases and monitor participant follow-up for trials.
• Use multiple data platforms including EHRs to analyze participant data.
• Support IRB policies and verify required study data with team.

Skills

EPIC

Medidata Rave

REDCap

EPIC SlicerDicer

Data management

Oncology terminology

Electronic medical records

Education

Bachelor's degree preferred

Tools

EPIC software

Medidata Rave

REDCap

SlicerDicer

Job description

Trinity Health Of New England is seeking a detail-oriented Clinical Research Data Assistant to support our Oncology Clinical Research Program. This role focuses on accurate collection, management, analysis, and reporting of clinical research data to ensure compliance with protocols, regulatory requirements, and sponsor expectations.

The role requires collaboration with Clinical Research Coordinators, investigators, healthcare providers, and sponsors to maintain data integrity across oncology