Sr. Clinical Research Associate

ICON Strategic Solutions; Oregon; On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Health and wellbeing programmes

Retirement plans

Learning and development opportunities

Competitive base salary

Job summary

ICON Strategic Solutions in Oregon is seeking a Senior Clinical Research Associate to oversee the monitoring of clinical trial sites, ensuring studies are conducted in accordance with the protocol, ICH GCP, and applicable regulatory requirements. This role emphasizes end-to-end site oversight and collaboration with cross-functional teams.

You will conduct site qualification, initiation, monitoring, and close-out visits, review data for accuracy, and collaborate with cross-functional teams to

Qualifications

• A degree in life sciences, nursing, or a related discipline.
• Proven experience working as a Clinical Research Associate.
• Strong knowledge of ICH GCP and applicable regulatory requirements.
• Ability to manage multiple sites and priorities independently.
• Willingness to travel in line with study requirements.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close out visits
• Ensure investigator site compliance with study protocols, ICH GCP, and regulatory requirements
• Review clinical data for accuracy, completeness, and consistency
• Identify site level risks and support corrective and preventive actions
• Maintain high quality monitoring documentation and reports
• Build effective working relationships with investigators and site staff
• Collaborate with cross functional study teams to support trial delivery

Skills

Clinical research experience

Site management

Regulatory knowledge

Travel readiness

Education

Bachelor's degree in life sciences or nursing or related discipline

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 Clinical Research Associate at ICON, you will be responsible for the monitoring and oversight of clinical trial sites, ensuring studies are conducted in accordance with the protocol, ICH GCP, and applicable regulatory requirements.

What You Will Do:

In this role you will be responsible for the end-to-end monitoring and oversight of clinical trial sites.

Key responsibilities include:

• Conduct site qualification, initiation, monitoring, and close out visits
• Ensure investigator site compliance with study protocols, ICH GCP, and regulatory requirements
• Review clinical data for accuracy, completeness, and consistency
• Identify site level risks and support corrective and preventive actions
• Maintain high quality monitoring documentation and reports
• Build effective working relationships with investigators and site staff
• Collaborate with cross functional study teams to support trial delivery

Your Profile:

To succeed in this role, you will bring strong clinical research experience and a proactive approach to quality and compliance.

Required qualifications and experience:

• A degree in life sciences, nursing, or a related discipline
• Proven experience working as a Clinical Research Associate
• Strong knowledge of ICH GCP and applicable regulatory requirements
• Ability to manage multiple sites and priorities independently
• Willingness to travel in line with study requirements

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.