CRA II and Senior CRA

ICON plc; Portland (OR); On-site; USD 75,000 - 115,000; Full time

Job summary

Join a forward-thinking clinical research organization as a Senior Clinical Research Associate. In this pivotal role, you will lead the design and analysis of clinical trials, ensuring data integrity and patient safety while collaborating with investigators. This dynamic position offers the chance to contribute to groundbreaking treatments in a supportive and inclusive environment. With a commitment to diversity and innovation, this organization values your expertise and provides opportunities for professional growth. If you're passionate about advancing healthcare and thrive in a collaborative setting, this role is an exciting opportunity to make a significant impact.

Benefits

Health Insurance

Retirement Planning

Life Assurance

Flexible Benefits

Employee Assistance Programme

Qualifications

• 2.5+ years of independent field monitoring experience required.
• In-depth knowledge of ICH-GCP guidelines and clinical trial regulations.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits.
• Ensure protocol compliance and patient safety throughout the trial.

Skills

Clinical Trial Processes

Data Integrity

Communication Skills

Organizational Skills

Monitoring Experience

Education

Bachelor's Degree in Scientific or Healthcare-related Field

Job description

Senior CRA - West Coast/Central U.S. (Oncology, Obesity, GI, Cardio, Endo a plus)

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.

We are currently seeking a Senior CRA to join our diverse and dynamic team. As a Senior Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

1. Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
2. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
3. Collaborating with investigators and site staff to facilitate smooth study conduct.
4. Performing data review and resolution of queries to maintain high-quality clinical data.
5. Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

Your profile

1. Bachelor's degree in a scientific or healthcare-related field.
2. Experience monitoring Oncology, Obesity, and/or Gastrointestinal studies.
3. Minimum of 2 ½ years of independent field monitoring experience – all types of visits.
4. Ability and willingness to travel at least 60% per month.
5. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
6. Strong organizational and communication skills, with attention to detail.
7. Ability to work independently and collaboratively in a fast-paced environment.

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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others.

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. 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.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply.