CRA II and Senior CRA

ICON; Portland (OR); Remote; USD 60,000 - 100,000; Full time

Job summary

Join a forward-thinking organization as a Clinical Research Associate II, where you will play a crucial role in the design and analysis of clinical trials. This position offers the opportunity to work on innovative treatments while ensuring the highest standards of patient safety and data integrity. You will collaborate with a diverse team, contributing to groundbreaking studies in Oncology and other fields. With a commitment to fostering an inclusive environment, this role not only promises personal growth but also the chance to make a significant impact in the healthcare industry. Embrace this exciting opportunity to advance your career in clinical research.

Benefits

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Qualifications

• Minimum of 2 years experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes and ICH-GCP guidelines.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits.
• Ensure protocol compliance and data integrity throughout the trial process.
• Collaborate with investigators and site staff for smooth study conduct.

Skills

Clinical Trial Monitoring

Data Integrity

Patient Safety

Oncology Studies

Communication Skills

Organizational Skills

Education

Bachelor's degree in a scientific or healthcare-related field

Job description

CRA II and Senior CRA - ONCOLOGY - Home-based in CENTRAL U.S. and 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.

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II 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 years of experience as a Clinical Research Associate.
4. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
5. Strong organizational and communication skills, with attention to detail.
6. 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:

1. Various annual leave entitlements.
2. A range of health insurance offerings to suit you and your family’s needs.
3. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
4. 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.
5. Life assurance.
6. 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, 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 here.

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.