Sr. CRA - Oncology

ICON Strategic Solutions; California; Presencial; USD 90.000 - 120.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes

Learning and development opportunities

Descripción de la vacante

ICON Strategic Solutions is seeking a Senior Clinical Research Associate - Oncology for the West Coast. This sponsor-dedicated role leverages ICON's global expertise to monitor trials, ensure quality, and drive continuous improvement.

You will lead monitoring tasks, perform site visits, and collaborate with cross-functional teams to ensure accurate data collection and reporting. Expect frequent travel (~60%) as you support site staff and drive trial execution.

Formación

• Monitoring practices, data integrity and site management.
• Excellent communication, interpersonal and stakeholder management skills.
• Willingness to travel approximately 60%.

Responsabilidades

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and GCP standards.
• Conducting site visits to assess site performance and resolve issues.
• Collaborating with cross-functional teams to ensure timely data collection and reporting.
• Providing training and guidance to site staff and other CRAs.

Conocimientos

Clinical trial monitoring

Regulatory knowledge

Site management

Data integrity

Communication

Educación

Bachelor's degree in a relevant scientific discipline

Herramientas

Clinical trial software

Descripción del empleo

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- 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.