In-house Clinical Research Associate II - Oncology
Worldwide Clinical Trials · Virtual United States North Carolina
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Worldwide Clinical Trials seeks an experienced Clinical Research Associate II to manage oncology study sites in compliance with GCP standards and regulations. The role involves coordinating site activities, monitoring data quality, supporting field teams, and mentoring junior staff across virtual operations.
What they're looking for
- Bachelor's degree in medical, biological, physical, health, pharmacy, or related science
- Minimum two years clinical research experience (study coordinator, research nurse, or equivalent)
- Demonstrated oncology clinical trial experience
- Strong written and oral communication abilities
- Proficiency with Microsoft Office and familiarity with IVRS and eCRF systems
- Working knowledge of FDA/EU regulations, ICH Guidelines, and GCP principles
What you'll be doing
- Manage site documentation, TMF/ISF maintenance, and quality control per GDP standards
- Conduct pre-study, initiation, interim, and closeout monitoring visits under CRA or CTM guidance
- Review EDC data for completion and accuracy; assist sites in resolving queries and data issues
- Coordinate study materials shipment, maintain site communication per monitoring plans
- Mentor in-house CRA team members and support recruitment, prescreening, and site staff changes
Key requirements
- Therapeutic area
- Oncology
Privacy & handoff
This role links to Worldwide Clinical Trials's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.