Senior Clinical Research Associate

ICON Strategic Solutions; Denver (NC); Hybrid; USD 111,000 - 138,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement plan

LifeWorks EAP

Life assurance

Flexible benefits

Job summary

ICON Strategic Solutions, a sponsor-dedicated FSP, seeks a Senior CRA for Colorado with oncology experience. You will monitor sites, conduct visits, and collaborate with cross‑functional teams to ensure accurate data collection and trial execution across multiple sites.

A strong regulatory background and ability to travel up to 60% are required. Join a global leader in clinical research support, offering career development and diverse benefits while contributing to treatments that benefit

Qualifications

• Advanced degree in life sciences, nursing, or medicine.
• Extensive experience as a Clinical Research Associate with strong regulatory knowledge.
• Proven ability to manage multiple sites and projects with strong organizational skills.

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 trial execution.
• Collaborate with cross-functional teams for timely data collection and reporting.
• Provide training and guidance to site staff to maintain high standards of conduct.
• Build and maintain relationships with site personnel and stakeholders to facilitate operations.

Skills

GCP knowledge

Site monitoring

Multi-site management

Regulatory compliance

Stakeholder management

Education

Advanced degree in life sciences

Tools

Clinical trial software

Job description

Senior CRA - Colorado - Oncology

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.

What You Will Be Doing

• 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

• Advanced degree in a relevant field such as life sciences, nursing, or medicine.
• 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.
• Must be located in the Colorado
• Oncology monitoring experience is required
• Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

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

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Salary range: $110,520.00-$138,150.00