Senior CRA, Phase I Oncology - West Coast (60% Travel)

ICON; United States; On-site; USD 111,000 - 138,000; Full time

Benefits offered by this job

Competitive salary

Health coverage

Retirement plan

Life insurance

Wellbeing resources

Career development

Job summary

ICON Strategic Solutions is seeking a Senior Clinical Research Associate (CRA) for Phase 1 Oncology on the West Coast. You will oversee monitoring activities in a sponsor-dedicated model, ensuring studies comply with protocols, GCP, and regulatory standards.

You will lead site visits, resolve issues, and collaborate with cross-functional teams to ensure accurate data collection and reporting. Travel approximately 60% is required, and candidates should have extensive CRA experience and strong

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare field.
• Extensive experience as a Clinical Research Associate with strong regulatory knowledge.
• Proven ability to manage multiple sites and projects concurrently with strong organizational skills.
• Expertise in monitoring, data integrity, and site management with software proficiency.
• Excellent communication and stakeholder management to drive compliance in a complex environment.
• Willingness to travel approximately 60%.

Responsibilities

• Monitor clinical trial sites to ensure adherence to protocols, GCP, and regulatory requirements.
• Perform site visits to assess performance, resolve issues, and support successful trial execution.
• Collaborate with cross-functional teams to ensure timely data collection and reporting.
• Provide training and guidance to site staff and other CRAs.
• Build and maintain relationships with site personnel and stakeholders for smooth operations.

Skills

Clinical trial monitoring

Site management

Data integrity

Regulatory knowledge

Communication

Travel readiness

Education

Bachelor's degree in science/healthcare

Tools

Clinical trial software

Job description

ICON Strategic Solutions is seeking a Senior Clinical Research Associate (CRA) for Phase 1 Oncology on the West Coast. You will oversee monitoring activities in a sponsor-dedicated model, ensuring studies comply with protocols, GCP, and regulatory standards.

You will lead site visits, resolve issues, and collaborate with cross-functional teams to ensure accurate data collection and reporting. Travel approximately 60% is required, and candidates should have extensive CRA experience and strong