About Accelagen

We are a leading, locally positioned and globally adept Clinical Research Organisation (CRO) headquartered in Australia working with innovative clients across the globe to make a tangible impact on the future of human health and wellness. With over a decade of delivered success, our experience is widely varied across the health, wellness and disease spectrum. We offer end-to-end services across Strategic Consultants, Clinical Trials, Regulatory Affairs & Biometrics.

About the Role

We're looking for a Statistical Programmer to join our growing Biostatistics team and help deliver high-quality clinical trial data, analyses, and reporting that supports the development of life-changing therapies.

Reporting to the Principal Statistical Programmer, you'll be responsible for programming, validating, and delivering clinical trial datasets and statistical outputs that meet regulatory, quality, and client requirements. You'll work closely with Biostatistics, Data Management, Project Management, and sponsors to ensure accurate and timely study deliverables.

Key Responsibilities

- Program and validate clinical trial datasets and outputs using SAS.
- Develop and review programming documentation, including annotated CRFs, reviewer guides, and define.xml files.
- Deliver CDISC compliant datasets and study outputs.
- Perform quality control and validation of programs, logs, and outputs.




- Collaborate with cross-functional study teams and contribute to project delivery.
- Support continuous improvement initiatives and programming standards.
- Maintain current knowledge of industry trends, GCP, and regulatory requirements.

About You You are a proactive, detail-oriented programmer with a passion for quality and problem-solving. You thrive in a collaborative environment and enjoy contributing to the successful delivery of clinical trials.

You'll bring:

- A degree in Statistics, Life Sciences, Computer Science, or a related discipline.
- Strong SAS programming skills.
- Experience working with clinical trial data and CDISC standards.
- Knowledge of ICH-GCP and regulatory requirements.
- Excellent communication and stakeholder management skills.
- At least 2 years' experience in clinical trial statistical programming.
- CRO experience and SAS certification will be highly regarded.

Why Accelagen?

- Adaptable and hybrid working arrangements.
- A collaborative, supportive, and values-driven culture.
- Exposure to a diverse portfolio of clinical studies and clients.
- Ongoing learning and professional development opportunities.
- The prospect to make a meaningful impact on clinical research and patient outcomes.

Ready to take the next step in your clinical programming career? Apply now and join Accelagen in advancing research that improves lives.

📌 Statistical Programmer (Hawthorn)
🏢 Accelagen
📍 Hawthorn