CRA II and Senior CRA

ICON plc; Long Beach (CA); On-site; USD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a Clinical Research Associate to oversee early phase oncology trials. In this crucial role, you'll ensure compliance with protocols and regulatory standards while maintaining data integrity and participant safety. You'll monitor clinical trial sites, conduct site visits, and collaborate with cross-functional teams to drive successful trial execution. With a commitment to diversity and inclusion, this innovative firm offers a supportive work environment and competitive benefits, making it an exciting opportunity for those passionate about clinical research and patient care.

Benefits

Various annual leave entitlements

Health insurance offerings

Retirement planning

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Qualifications

• Experience in monitoring early phase oncology clinical trials.
• Strong understanding of clinical trial processes and regulatory requirements.

Responsibilities

• Monitor clinical trial sites for adherence to protocols and GCP standards.
• Conduct site visits to assess performance and resolve issues.
• Collaborate with teams for accurate data collection and reporting.

Skills

Monitoring clinical trials

Regulatory compliance

Data integrity

Interpersonal skills

Problem-solving

Stakeholder management

Education

Bachelor's degree in life sciences, nursing, or medicine

Tools

Clinical trial software

Job description

CRA II or Senior CRA early phase oncology (home-based)

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 CRA II or Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a 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:

• 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:

• Bachelor's degree in a relevant field such as life sciences, nursing, or medicine.
• Experience in monitoring early phase clinical trials.
• Must have recent expertise monitoring ONCOLOGY clinical trials.
• 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.

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.