Sr. CRA
On-site · Houston, Texas, United States or Dallas, Texas, United States
Job Summary
Senior CRA to oversee and manage oncology clinical trial monitoring at ICON, leading site visits and ensuring adherence to study protocols, regulatory requirements, and GCP. Responsibilities include monitoring sites, resolving issues, collaborating with cross-functional teams for timely data collection and reporting, providing training to site staff, and building strong relationships with site personnel to facilitate smooth trial operations. Requires a bachelor's degree, extensive CRA experience, strong monitoring and data integrity expertise, ability to manage multiple sites, travel ~60%, and legal right to work in the U.S. ICON offers competitive compensation and comprehensive benefits.
Required Qualifications
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate
- Strong understanding of clinical trial processes and regulatory requirements
- Proven ability to manage multiple sites and projects
- Expertise in monitoring practices, data integrity, and site management
- Proficiency in relevant clinical trial software and tools
- Excellent communication, interpersonal, and stakeholder management skills
- Experience monitoring oncology studies
- Willingness to travel approximately 60%
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