Sr. CRA

ICON Strategic Solutions; Portland (OR); On-site; USD 90,000 - 130,000; Full time

Job summary

ICON Strategic Solutions is seeking a Senior CRA to oversee and manage clinical trial activities, ensuring compliance with protocol, regulatory requirements, and industry standards. Travel is up to 50% and oncology monitoring experience is required.

You will lead monitoring tasks with technical depth, focusing on quality and continuous improvement, while collaborating with cross-functional teams to ensure timely data collection and reporting.

Qualifications

• 4+ years of independent monitoring experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
• Oncology monitoring experience required.
• Bachelor's degree preferred (degree not required)

Responsibilities

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

Skills

Monitoring

GCP knowledge

Regulatory knowledge

Travel readiness

Oncology monitoring

Education

Bachelor's degree

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.

As a Senior CRA at ICON, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. Travel is up to 50% and there are no required days on site metrics. Oncology monitoring experience required.

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 preferred (degree not required)
• 4+ years of independent monitoring experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
• Oncology monitoring experience required
• Willingness to travel as required (approximately 50%)

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

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.