Principal Statistical Programmer

About our business

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.

Are you ready to grow your career?

We have an opportunity to join as a Statistical Programmer (II, Senior or Principal).

If you're looking for a shared learning environment and a genuine close-knit team, then here is your chance. Accelagen has a positive working culture and push for shared-learning and upskilling, so it's a great opportunity for anyone looking to develop cross-functional skills.

With plans for growth in the coming years, there are strong career progression opportunities, including tailored development pathways aligned with your goals.

In this role, you'll work on full end-to-end clinical trials across a range of therapeutic areas, including oncology. Experience with ADaM and SDTM is essential.

This opportunity is well-suited to candidates with 12+ months of clinical statistical programming experience in a CRO.

KEY RESPONSIBILITIES

• Craft and validate SAS programs for comprehensive analysis and reporting of clinical trial data.
• Collaborate intricately with statisticians, data managers, and peers to devise detailed statistical analysis plans.
• Maintain meticulous documentation, ensuring adherence to regulatory standards and quality benchmarks.
• Implement rigorous quality control measures to uphold data precision and uniformity.
• Contribute to streamlining and enhancing standard programming procedures and tools.
• Keep abreast of industry advancements, driving continuous enhancement.

DESIRED SKILLS:

• Hold a Bachelor's or Master's degree in statistics, computer science, or related fields.
• Demonstrated expertise as a Clinical Statistical SAS Programmer within pharmaceutical, biotech, or clinical research sectors.
• Proficiency in SAS programming, covering Base SAS, SAS/STAT, SAS Macro, and SAS/GRAPH.
• Strong familiarity with CDISC standards and regulatory frameworks governing clinical trial data.

We are looking for candidates all across Australia, NSW preferred. If this sounds like the right fit for you, please apply today

Job Types: Full-time, Permanent

Pay: $130,000.00 – $140,000.00 per year

Benefits:

• Employee mentoring program
• Professional development assistance
• Referral program
• Work from home

Work Location: Hybrid remote in Hawthorn East VIC 3123