Principal/Senior Statistical Programmer (SAS) / Australian CRO / Remote AU
An opportunity to join a growing Contract Research Organisation. This company have been around for 15 years and so are established and stable with a strong stamp in the industry - partnering with multiple biotech & pharma sponsors.
You will be leading multiple projects in early-phase clinical trials. They have a close team here in Australia and offer a shared learning environment with L&D development plans in place to ensure employees are upskilled in areas of interests.
Looking for an experienced SAS Programmer with at least 3 years' experience and acted as project lead. Must have specific clinical trial experience from a CRO or Pharma and have expert CDISC knowledge.
Position Overview: Principal Statistical Programmer
- Lead and oversee programming activities, ensuring the successful execution of projects from inception to completion.
- Collaborate with cross-functional teams on the development of statistical analysis plans, programming specifications, and the production of high-quality deliverables.
- Implement rigorous quality control processes to ensure accuracy and reliability of statistical outputs, adhering to regulatory standards.
- Utilize your advanced programming skills in SAS and other relevant tools to analyze and report clinical trial data.
- Work closely with biostatisticians, data managers, and other team members to ensure seamless integration of programming activities within the overall project timeline.
- Bachelor's or higher degree in Computer Science, Statistics, or a related field.
- Minimum of 3 years of experience in statistical programming within the pharmaceutical or CRO industry.
- Proficient in SAS programming and other relevant programming languages, with a solid understanding of CDISC standards.
- Title: Principal SAS Programmer
- Location: Remote, Australia
- Salary: Around $130,000 - $160,000 plus superannuation (this is dependent on experience and open to negotiation for the right candidate
If you are excited about the prospect of shaping statistical programming strategies for clinical trials and leading a talented team, please apply direct or submit your resume to Keeley at (cover-letters are not necessary - we value your time).