Job Description

Looking for your next move - but want something different from traditional CRO life?

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We're working with a leading global CRO that is expanding its Australian FSP team and is looking for experienced CRA II and Senior CRAs across Sydney, Melbourne, Brisbane and Adelaide.

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This is an chance to move into an FSP model, where you remain employed by the CRO but work closely with a dedicated sponsor team - giving you the scale and security of a global organisation alongside a much more focused day-to-day experience.

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Why consider an FSP?

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Work closely with one sponsor

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Rather than constantly moving between different sponsors and projects, you'll have the opportunity to develop a deeper understanding of your sponsor, their processes and their clinical development programmes.

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Build real sponsor-side exposure

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You'll work as an extension of the sponsor's clinical team, giving you valuable insight into how a global pharmaceutical organisation operates.

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International study exposure

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Work on global clinical trials alongside international teams, with exposure to complex protocols and high-quality clinical research.

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More consistency

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The FSP model can provide greater continuity than traditional CRO project work, allowing you to become embedded within a team and build strong relationships.

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You'll have the backing of a major CRO with established systems, technology, training, career frameworks and resources.

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Whether your goal is to progress further as a Senior CRA, move towards Clinical Project Management, or explore other areas of clinical operations, you'll have access to structured development opportunities within a large global organisation.

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What you'll be doing

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- Conducting monitoring activities across assigned clinical trials
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- Managing site relationships and supporting sites throughout the study lifecycle
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- Ensuring compliance with the protocol, ICH-GCP and applicable regulations
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- Performing SIVs, IMVs and close-out activities
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- Identifying and resolving site issues
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- Supporting study start-up and site activation activities where required
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- Working closely with the sponsor's clinical operations team
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- Maintaining high-quality documentation and trial records
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- Contributing to a collaborative, international study team
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What we're looking for

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CRA II

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- Previous CRA experience within a CRO, sponsor or similar clinical research environment
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- Experience independently managing monitoring activities (12 months+)
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- Strong understanding of ICH-GCP and clinical trial processes
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- Excellent communication and stakeholder management skills
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- Ability to work autonomously while contributing to a wider team
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Senior CRA

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- Strong independent monitoring experience (4 years+)
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- Experience across complex clinical trials
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- Confidence managing site relationships and resolving issues
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- Robust understanding of clinical trial regulations and GCP
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- Ability to act as a trusted clinical contact for sites and study teams
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- Previous experience mentoring or supporting junior CRAs is advantageous
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The opportunity

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If you enjoy clinical research but are looking for more consistency, closer sponsor interaction and the opportunity to become genuinely embedded within a global study team, an FSP environment could be a great next step.

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Locations:

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Sydney | Melbourne | Brisbane | Adelaide

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Level:

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CRA II / Senior CRA

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Study exposure:

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International clinical trials

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For a confidential discussion, get in touch to learn more about the sponsor, studies and FSP structure.

📌 Clinical Research Associate (Victoria)
🏢 i-Pharm Consulting
📍 Victoria