# CRA II, Australia - WA Remote

**Company**: ICON Strategic Solutions
**Location**: Sydney
**Work arrangement**: remote
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Australia-Sydney/CRA-II---Senior-CRA_JR164266?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/cra-ii-australia-wa-remote-08eaee6a-fc7/

## Description

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.

As a CRA II at ICON, you will perform site qualification, initiation, monitoring and closeout activities as assigned.

**Responsibilities** You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

- Perform site qualification, initiation, monitoring and closeout activities as assigned.

- Verify protocol, GCP and regulatory compliance and participant protection.

- Review source data, essential documents and site processes for accuracy and completeness.

- Identify and follow up findings, risks and corrective actions.

- Maintain clear communication with investigators, site staff and study teams.

**Required qualifications and experience**

- Relevant life sciences, healthcare or clinical research qualification, or equivalent relevant clinical research experience.

- Minimum of 2 years of experience as a Clinical Research Associate.

- In-depth knowledge of clinical trial processes, regulations, and ICH Good Clinical Practice (GCP) guidelines.

- Knowledge of ICH Good Clinical Practice (GCP), clinical trial conduct and site monitoring requirements.

- Practical experience with site monitoring or site management appropriate to the level of role.

- Experience performing site qualification, initiation, monitoring and closeout activities as assigned.

- Experience verifying protocol, GCP and regulatory compliance and participant protection.

**Preferred qualifications and experience**

- Therapeutic area expertise relevant to assigned studies.

- Experience with risk-based monitoring or centralised monitoring approaches.

- Experience with clinical trial management systems (CTMS), electronic data capture (EDC) and electronic trial master file systems.

**Working conditions**

- Willingness to travel as required (approximately 60%).

**Rewards & Benefits** ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

- Competitive base salary and performance-related incentives

- Health and wellbeing programmes including medical, dental, and vision coverage where applicable

- Retirement and pension plans

- Life assurance and disability coverage

- Employee assistance programmes and wellbeing resources

- Learning and development opportunities through structured training and career pathways

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## Skills

### Required
- clinical trial processes
- ICH Good Clinical Practice (GCP)
- site monitoring
- clinical research

### Nice to have
- risk-based monitoring
- centralised monitoring approaches
- CTMS
- EDC
- electronic trial master file systems

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Australia-Sydney/CRA-II---Senior-CRA_JR164266?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)