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About the Role
Lead complex clinical study programming projects, owning the programming lifecycle and driving innovation in programming efficiency. Collaborate with cross-functional teams, mentor junior programmers, and ensure regulatory compliance.
Responsibilities
- Plan, coordinate, and oversee programming activities for complex clinical studies.
- Serve as Programming Team Lead for assigned projects.
- Own the programming lifecycle from database integration to statistical outputs.
- Design and implement advanced macros, tools, and process improvements.
- Collaborate with statisticians, data managers, and clients.
- Provide technical expertise and innovative solutions to complex project challenges.
- Share expertise with junior programmers.
- Ensure all deliverables meet regulatory standards and internal quality benchmarks.
- Develop and maintain programming specifications, documentation, and other study-related deliverables.
Requirements
- A degree in Computer Science or a related field (Master’s preferred).
- 3 to 5 years of experience in statistical programming within clinical trials.
- Advanced SAS programming skills (Base SAS, SAS Graph, SAS Macro).
- Experience with R programming and ADNCA for PK analysis will be considered an asset.
- Strong understanding of clinical data, statistical principles, and regulatory requirements.
- Advanced knowledge of CDISC standards (SDTM and ADaM).
- Excellent communication, leadership, and multitasking abilities.
- Demonstrated ability to independently solve complex technical challenges, lead technical initiatives, and adapt to evolving tools, technologies, and industry standards.
- Candidates requiring sponsorship to work in Australia cannot be considered.
Skills
- SAS programming
- SAS Graph
- SAS Macro
- R programming
- ADNCA for PK analysis
- CDISC standards (SDTM and ADaM)
- Clinical data analysis
- Statistical principles
- Regulatory requirements
- Communication
- Leadership
- Multitasking
Location
- Australia
Work Type
- Full-time
Experience Level
- Mid-level
Education Level
- Master's degree preferred
- Bachelor's degree
About the Company
- IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
- We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
- Learn more at https://jobs.iqvia.com
Equal Opportunity
- IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.