In this role, you'll thrive in a collaborative environment, working alongside seasoned professionals boasting decades of industry expertise. You'll have the opportunity to enhance your skills within a culture of shared learning and development.
Being a smaller business, you will have full responsibility of the entire clinical process from start to finish, partnering closely with cross-functional teams, and providing end-to-end programming initiatives. Your contributions will ensure the seamless execution of projects, delivering to small biotech sponsors.
As you manage multiple clinical trials, you'll wear various hats, fostering a sense of versatility and progression within a tight-knit team setting.
They are hiring for a Programmer I, Programmer II or Senior Programmer with solid clinical trial experience.
Role Highlights
- Develop and validate SAS programs for analysis and reporting of clinical trial data.
- Collaborate closely with statisticians, data managers, and peers to craft comprehensive statistical analysis plans.
- Maintain meticulous documentation to ensure regulatory compliance and quality assurance.
- Uphold stringent quality control measures to guarantee data accuracy and consistency.
- Contribute to refining and optimising standard programming processes and tools.
- Stay abreast of industry trends and best practices to drive continuous improvement.
- Bachelor's or Master's degree in statistics, computer science, or a related discipline.
- Proven track record as a Clinical Statistical SAS Programmer within pharmaceutical, biotechnology, or clinical research realms.
- Proficiency in SAS programming, encompassing Base SAS, SAS/STAT, SAS Macro, and SAS/GRAPH.
- Strong grasp of CDISC standards and regulatory prerequisites governing clinical trial data.
- Position: SAS Programmer (II/Senior/Principal based on experience) *Salary: $110k - $145k depending on experience *Location: Remote, Australia