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SalaryA chance to join a dynamic, innovative CRO who are growing out their statistics department in Australia.
This role would suit an experienced SAS Programmer (II, Senior, Principal).
You will be collaborating with senior management and highly experienced Programmers, with decades of experience in their fields, and so will be a strong opportunity to upskill in a shared learning environment.
Due to their size, you will be covering the full end-to-end clinical process, working closely with cross-functional teams, data managers, and clinical researchers, to ensure the successful execution of projects and the delivery of accurate and timely results.
This company is a full service Australian CRO, who continue to grow out their presence across the country. You will be responsible for managing multiple clinical trials, working in a cross-functional 'wear all hats' type of role. This role presents multiple opportunity for progression working closely in a small team environment.
Suitable for an experienced Statistical (SAS) Programmer with over 2 years' experience leading trials.
ROLE RESPONSIBILITIES
Offering a permanent (full time) opportunity for an experienced Statistical Programmer, this role will be based fully remote across Australia.
- Develop and validate SAS programs for the analysis and reporting of clinical trial data.
- Collaborate with statisticians, data managers, and other team members to design and implement statistical analysis plans.
- Create and maintain documentation for statistical programming activities, ensuring compliance with regulatory standards.
- Perform quality control checks on datasets, tables, listings, and figures to ensure accuracy and consistency.
- Contribute to the development and improvement of standard programming processes and tools.
- Stay current with industry trends, guidelines, and best practices related to statistical programming.
- Bachelor's or Master's degree in statistics, computer science, or a related field.
- Proven experience as a Clinical Statistical (SAS) Programmer in the pharmaceutical, biotechnology, or clinical research industry.
- Proficiency in SAS programming, including Base SAS, SAS/STAT, SAS Macro, and SAS/GRAPH.
- Strong understanding of CDISC standards and regulatory requirements for clinical trial data.
*Salary: Depending on experience level $120k - $170k
*Location: Remote Australia
Apply direct or contact Keeley Munday on 02 8310 5854 / kmunday@i-pharmconsulting.com
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