Sr. CRA - Oncology and multi-ta

ICON Strategic Solutions; Los Angeles (CA); On-site; USD 110,000 - 150,000; Full time

Benefits offered by this job

Competitive salary

Health and wellbeing programmes

Retirement plans

Life insurance

Wellbeing resources

Training and career development

Job summary

ICON Strategic Solutions is seeking a Senior Clinical Research Associate for Oncology and Multi-TA on the West Coast. The role focuses on trial monitoring with emphasis on quality, GCP adherence, and continuous improvement across sites.

You will lead site visits, ensure data integrity, and train site staff while collaborating with cross functional teams to support timely trial execution and stakeholder management.

Qualifications

• Bachelor's degree in a relevant scientific or healthcare field.
• Extensive experience as a Clinical Research Associate with understanding of trial processes and regulatory requirements.
• Ability to manage multiple sites/projects with strong organization and problem solving.
• Expertise in monitoring practices, data integrity, and site management with relevant tools.

Responsibilities

• Monitor clinical trial sites to ensure adherence to protocols, regulatory requirements, and GCP.
• Conduct site visits to assess performance, resolve issues, and support trial execution.
• Collaborate with cross functional teams to ensure timely data collection and reporting.

Skills

Clinical trial monitoring

Regulatory compliance

Data integrity

Communication

Stakeholder management

Travel readiness

Education

Bachelor's degree in a relevant field

Tools

Clinical trial software

Job description

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.

Senior Clinical Research Associate - Oncology and Multi-TA/ West Coast

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

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.

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.

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.