Launch your career in Clinical Data Management.

PureCDM is seeking a motivated Clinical Data Associate to join our collaborative and supportive Clinical Data Management team.

This is an excellent opportunity for a graduate, early-career clinical research professional, Clinical Trial Coordinator, Study Coordinator or life sciences professional looking to build a career in clinical data management.

About PureCDM

PureCDM is a specialist biometrics organisation supporting clinical research clients with high-quality clinical data management, biostatistics and programming services.

We are practical, team-oriented, flexible and quality-focused, with a strong team spirit and a genuine commitment to developing our people.

About the Role

As a Clinical Data Associate, you will support Lead Data Managers and study teams with day-to-day clinical data management activities across clinical trial projects.

You will gain hands-on experience in study documentation, database testing, data review, reconciliation and maintaining study records for the Trial Master File.

What You’ll Be Doing

You will:

- Assist with study-specific documentation such as Data Management Plans, CRF Completion Guidelines and Manual Review Plans.
- Support User Acceptance Testing of database screens and edit checks.
- Perform manual data review to help ensure clinical trial data is complete, accurate and high quality.
- Assist with reconciliation of external data sources against the clinical trial database.
- Maintain project documentation for filing in the Trial Master File.
- Work closely with Lead Data Managers,



project teams and internal stakeholders to support smooth study delivery.

About You

You are curious, organised, detail-oriented and ready to learn. You enjoy working with data, asking questions, solving problems and being part of a supportive team.

You may be a recent graduate or an early-career clinical research professional looking to move into clinical data management.

You will bring:

- A degree in life sciences, health sciences or a related field, or relevant clinical research experience.
- An interest in clinical trials, data quality and the drug development process.
- Strong attention to detail and good organisational skills.
- Effective communication skills and a collaborative working style.
- Ability to manage priorities, follow processes and meet deadlines.
- Prior experience as a Clinical Trial Coordinator, Study Coordinator, CRA, Clinical Data Associate or similar will be highly regarded.

Why Join PureCDM?

At PureCDM, you will be supported to learn, grow and build practical clinical data management skills.

You will have the opportunity to:

- Join a highly collaborative and supportive team that values team spirit.
- Learn from experienced clinical data management and biometrics professionals.
- Build hands‑on skills across clinical trial data management.
- Contribute to meaningful clinical research in a growing specialist organisation.
- Be part of a culture that values quality, ownership, development and shared success.

Ready to Start Your CDM Career?

If you are ready to build your career in clinical data management and contribute to high-quality clinical research, we would love to hear from you.

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📌 Clinical Data Associate I (Melbourne)
🏢 Purecdm
📍 Melbourne