Sr. CRA - Phase 1 Oncology West Coast

Regulatory Jobs; 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

Sr. CRA - Phase 1 Oncology West Coast

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.

As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. This position is sponsor dedicated and supporting Phase I Oncology trials.

What You Will Do:

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include:

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.

Required qualifications and experience:

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
• Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
• Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
• Willingness to travel as required (approximately 60%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Salary Range

$110,520.00-$138,150.00