In-house Clinical Research Associate II - CNS/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 site operations for oncology and CNS studies. The role involves coordinating study materials, monitoring data quality, conducting site visits, and mentoring junior team members while ensuring compliance with GCP and regulatory standards.
What they're looking for
- Bachelor's degree in medical, biological, physical, health, pharmacy, or related science
- Minimum two years clinical research experience in roles such as study coordinator or research nurse
- Demonstrated experience in both oncology and CNS/neurology therapeutic areas
- Understanding of FDA, EU Directive regulations, ICH Guidelines, and local requirements
- Proficiency with Microsoft Office and electronic data capture systems
- Strong oral and written communication with planning and organizational skills
What you'll be doing
- Coordinate study material shipment and receipt; maintain Trial Master File and Investigator Site File documentation
- Conduct pre-study, initiation, interim, and closeout monitoring visits under field CRA guidance
- Review electronic data capture CRFs for completion and compliance; assist sites with query resolution
- Generate reports and trackers from study portals and EDC systems for project team distribution
- Provide mentoring and training to in-house CRA team members; serve as operational point of contact for assigned studies
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.