Senior CRA

ICON plc; Portland (OR); Remote; USD 70,000 - 110,000; Full time

Job summary

An established industry player in healthcare intelligence is seeking a Senior Clinical Research Associate to oversee and manage clinical trial activities. This role is pivotal in ensuring compliance with regulatory requirements and maintaining data integrity throughout the study lifecycle. You will collaborate with cross-functional teams, conduct site visits, and provide training to site staff, all while fostering strong relationships with stakeholders. Join a diverse and dynamic team where your contributions will shape the future of clinical development and enhance the well-being of participants. This is an exciting opportunity to make a significant impact in the clinical research field.

Benefits

Health Insurance

Retirement Planning

Global Employee Assistance Programme

Life Assurance

Flexible Optional Benefits

Qualifications

• Extensive experience as a Clinical Research Associate with strong understanding of trial processes.
• 3 years of independent monitoring experience and expertise in data integrity.

Responsibilities

• Monitor clinical trial sites for adherence to protocols and GCP standards.
• Conduct site visits and collaborate with teams for data collection.

Skills

Clinical Trial Management

Regulatory Compliance

Data Integrity

Interpersonal Skills

Problem-Solving Skills

Communication Skills

Education

Advanced degree in life sciences, nursing, or medicine

Tools

Clinical Trial Software

Job description

Senior CRA- Central/West/East-Remote

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 Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing:

1. Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
2. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
3. Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
4. Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
5. Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

1. Advanced degree in a relevant field such as life sciences, nursing, or medicine.
2. Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
3. Located in the Central, West or East regions.
4. 3 years of independent monitoring experience.
5. Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
6. Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
7. Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex 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, 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.

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.