Clinical Trials Data Steward

University of California - Davis; Sacramento (CA); Hybrid; USD 50,000 - 80,000; Full time

Benefits offered by this job

Medical plans

Dental and vision coverage

Retirement plans

Paid time off

Continuing Education allowance

Job summary

UC Davis Comprehensive Cancer Center is seeking a Data Research Coordinator to support oncology clinical trials. You will manage data collection, ensure quality, and coordinate with investigators and sponsors to meet regulatory standards.

The role emphasizes data integrity, documentation, and timely reporting within a hybrid work model. A background in clinical research and knowledge of trial regulations are essential for success.

Qualifications

• Minimum of a high school diploma or GED with relevant experience.
• At least 2 years of clinical research coordinator experience.
• Familiarity with FDA and OHRP regulations is essential.
• Regulatory processes and data management knowledge for clinical trials.
• Ability to interpret medical records and physician notes.
• Proficiency with Microsoft Word, Excel, Outlook, Access.
• Strong tracking, recordkeeping and reporting skills.
• Excellent written and verbal communication and attention to detail.

Responsibilities

• Coordinate data collection and submission to study sponsors.
• Ensure data accuracy and quality through QA processes.
• Maintain and update study CRFs and EDC entries.
• Communicate with investigators, sponsors, and regulatory bodies.
• Support compliance with IRB, FDA, and NCI guidelines.
• Assist with data integrity and risk assessment for protocols.

Skills

Data management

Clinical research

Microsoft Office

Analytical thinking

Communication

Documentation

Education

High School or equivalent

2+ years clinical research coordinator experience

Bachelor's degree (preferred)

Tools

EDC systems

OnCore

MS Access

Job description

UC Davis Comprehensive Cancer Center is seeking a Data Research Coordinator to support oncology clinical trials. You will manage data collection, ensure quality, and coordinate with investigators and sponsors to meet regulatory standards.

The role emphasizes data integrity, documentation, and timely reporting within a hybrid work model. A background in clinical research and knowledge of trial regulations are essential for success.