About the Role
This role involves managing clinical trial data through a Clinical Trial Management System, supporting study coordination, data integrity, and system optimization for research operations.
Responsibilities
- Maintain and update clinical trial data within the CTMS platform
- Collaborate with research teams to ensure accurate study documentation
- Support user access and permissions within the system
- Generate reports for trial progress and enrollment metrics
- Assist in system configuration for new clinical studies
- Ensure compliance with data governance policies
- Troubleshoot CTMS-related issues and provide user support
- Participate in system upgrades and enhancements
- Train clinical staff on CTMS functionality and best practices
- Track protocol milestones and study timelines
- Validate data entries for consistency and completeness
- Coordinate with IT teams on system integrations
- Maintain audit-ready documentation for all system activities
- Monitor data quality and recommend process improvements
- Support regulatory inspection readiness activities
Nice to Have
- Experience with specific CTMS platforms such as OpenClinica or Medidata
- Prior work in oncology or specialty pharmacy research
- Certification in clinical research or data management
- Familiarity with electronic data capture systems
- Project management experience in healthcare settings
Compensation
Competitive salary and benefits package offered
Work Arrangement
Remote position within the United States
Team
Part of the clinical research technology team supporting data management and systems operations
Why This Role Matters
This position plays a key role in ensuring clinical trial data is accurately captured, managed, and reported, directly impacting research outcomes and patient care advancements.
What to Expect
You will work remotely with a team focused on research technology, supporting multiple clinical trials through system management, data oversight, and cross-functional collaboration.
Not available for this position
