Senior Clinical Research Associate

ICON; California City (CA); On-site; USD 111,000 - 138,000; Full time

Job summary

ICON seeks a Senior Clinical Research Associate to oversee Phase I Oncology trials across multiple sites in a sponsor-dedicated model. You will ensure protocol adherence, regulatory compliance, and data integrity while mentoring junior staff.

Travel approximately 60% is required, with focus on site monitoring, issue resolution, and timely data reporting across cross-functional teams. Strong communication and stakeholder management are essential.

Qualifications

• Bachelor's degree in a relevant scientific or healthcare discipline.
• Extensive Clinical Research Associate experience with strong clinical trial process knowledge.
• Ability to manage multiple sites and projects concurrently.
• Expertise in monitoring, data integrity, and site management.
• Current oncology monitoring experience required.
• Willingness to travel approximately 60%.
• Strong communication and stakeholder management skills.

Responsibilities

• Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standard adherence.
• Conduct site visits to assess performance, resolve 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 relationships with site personnel and stakeholders for smooth trial operations.

Skills

Site monitoring

Data integrity

Regulatory compliance

Oncology monitoring

Stakeholder management

Communication skills

Education

Bachelor's degree in a relevant scientific or healthcare discipline

Job description

Senior Clinical Research Associate position in a sponsor-dedicated model supporting Phase I Oncology studies. The role involves overseeing clinical trial activities at multiple sites to ensure protocol adherence, regulatory compliance, and data integrity while mentoring junior staff.

Responsibilities

• Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standard adherence
• Conduct site visits to assess performance, resolve 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 relationships with site personnel and stakeholders for smooth trial operations

Requirements

• Bachelor's degree in relevant scientific or healthcare discipline
• Extensive Clinical Research Associate experience with strong clinical trial process knowledge
• Proven ability to manage multiple sites and projects concurrently
• Expertise in monitoring practices, data integrity, and site management
• Current oncology monitoring experience required
• Willingness to travel approximately 60%
• Strong communication and stakeholder management skills

Compensation: $110,520–$138,150 base