Senior Clinical Research Associate

ICON seeks a Senior Clinical Research Associate to oversee clinical trial monitoring activities at sponsor-dedicated sites, ensuring protocol adherence and regulatory compliance. The role requires extensive CRA experience, preferably in oncology Phase I trials, with ability to manage multiple sites and mentor junior staff across a multi-state region.

Responsibilities

• Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standards
• Conduct site visits to assess performance, troubleshoot issues, and provide operational support
• Collaborate with cross-functional teams on timely and accurate data collection and reporting
• Train and guide site staff and other CRAs on clinical trial conduct standards
• Build and maintain stakeholder relationships to facilitate trial operations and compliance

Requirements

• Bachelor's degree in scientific or healthcare-related field
• Extensive Clinical Research Associate experience with strong regulatory and trial process knowledge
• Demonstrated ability to manage multiple sites and projects simultaneously
• Expertise in monitoring practices, data integrity, and clinical trial software tools
• Strong communication and stakeholder management skills
• Willingness to travel approximately 60% as required
• Preferred oncology experience with Phase I trial background

Compensation: $110,520–$138,150 base