Clinical Data Coordinator I — Hybrid, 3 Days in Office

Job overview

The Clinical Data Coordinator I role is hybrid, with three days in the office, in Irving, TX. The annual hiring range is $64,000–$80,000. The role supports Caris Medical Affairs protocols and projects at Precision Oncology Alliance sites, contributing to research intended to improve oncology treatment and outcomes. The coordinator collects, abstracts, enters, and reviews clinical research data, maintaining data integrity and quality. The work supports reliable study analysis by resolving queries, tracking site completion, maintaining documentation, and following clinical research and privacy requirements.

What you'll do

• Abstract clinical data from source documentation
• enter data into study-specific EDC case report forms
• clean and verify data
• resolve data queries
• track site goals and form completion
• prioritize cases for analysis
• maintain study documentation
• perform database quality-control audits
• support GCP, FDA, IRB, and HIPAA requirements
• coordinate with research teams and investigative sites.

What we're looking for

Skills & competencies

clinical data

clinical research

oncology

edc systems

data quality

clinical protocols

gcp

hipaa

hybrid

3 days in office

irving tx

caris life sciences

full-time

Work arrangement

• Weekend coverage required

Benefits & perks

• Medical, dental, and vision coverage
• health and flexible spending accounts
• paid time off and holidays
• 401(k) match and financial planning tools
• disability coverage
• employee assistance program
• pet insurance
• legal assistance
• tuition assistance.

Why this role

Supports oncology clinical research data quality and may require occasional evenings and overtime; travel to multiple investigative sites may be required.

About the employer

Caris Life Sciences is hiring for this role. Industry: Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology). Sector: 54.