Senior Associate, Remote Insurance & Pi Litigation

People2People - Perth; Gold Coast City; Hybrid; AUD 90,000 - 135,000; Full time

Benefits offered by this job

Health insurance

Retirement planning

Life assurance

Well-being benefits

Annual leave

Job summary

ICON Plc is seeking a Senior Clinical Research Associate for a hybrid role on the Gold Coast, Australia. You will oversee and manage clinical trial activities to ensure adherence to protocol, regulatory requirements and industry standards, with a focus on quality and continuous improvement.

You will lead monitoring tasks, perform site visits, and collaborate with cross-functional teams to ensure accurate data collection and reporting. Significant travel (~60%) is expected as part of the role.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Extensive experience as a Clinical Research Associate with strong regulatory knowledge.
• Proven ability to manage multiple sites and projects with strong organizational skills.
• Experience with monitoring practices, data integrity and site management.
• Excellent communication and stakeholder management abilities.

Responsibilities

• Monitor clinical trial sites for protocol compliance, regulatory adherence and GCP standards.
• Conduct site visits to assess performance, resolve issues and support trial execution.
• Collaborate with cross-functional teams to ensure timely data collection and reporting.
• Provide training and guidance to site staff to uphold high conduct standards.
• Build and maintain relationships with site personnel and stakeholders to smooth operations.

Job description

CRA Australia - Hybrid
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. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. **What You Will Do:**
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.

• 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:**
You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. **Required qualifications and experience:**
+ Bachelor's degree in a relevant scientific discipline or healthcare‑related field.
+ 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.
+ Willingness to travel as required (approximately 60%).

**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.

**Key Accountabilities:**
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