Principal Statistical Programmer

Roles and responsibilities

AL Solutions are looking for a highly skilled Senior or Principal Statistical Programmer to join a global, fast-paced organization committed to delivering innovative solutions in the clinical research space. This position offers the opportunity to play a critical role in supporting statistical programming activities across a range of clinical trials, ensuring quality and timely deliverables for clients worldwide.

Key Responsibilities:

• Lead the programming aspects of clinical trials, including the development of datasets (SDTM, ADaM) and statistical outputs (tables, listings, and figures).
• Provide technical expertise and leadership in developing and validating SAS programs in support of clinical trial analysis.
• Collaborate with biostatisticians, data managers, and other key stakeholders to deliver high-quality statistical outputs in line with regulatory requirements.
• Ensure adherence to industry standards (CDISC), company SOPs, and regulatory guidelines throughout all stages of clinical trial programming.
• Mentor and guide junior programmers, offering technical support and fostering a collaborative working environment.
• Oversee the successful delivery of programming deliverables on multiple projects, ensuring timelines are met while maintaining high standards of accuracy and quality.
• Participate in the development of programming tools and processes to optimize efficiency and quality.
• Competitive salary with performance-based bonus.
• Flexible working arrangements with opportunities for career growth and development.
• A collaborative and supportive work environment with a focus on innovation and professional development.

• This is an exciting opportunity for an experienced Statistical Programmer looking to take on a leadership role within a global organization. If you’re passionate about statistical programming and ready for your next challenge, we’d love to hear from you! Apply today.

Desired candidate profile

Qualifications:

• Bachelor’s degree in Statistics, Computer Science, or a related field (Master’s degree preferred).
• A minimum of 5 years of statistical programming experience in the pharmaceutical, biotech, or CRO industry.
• Advanced SAS programming skills and experience with clinical data standards (CDISC, SDTM, ADaM).
• Strong understanding of statistical principles, clinical trial design, and regulatory submission requirements.
• Excellent problem-solving skills with attention to detail and a proactive approach to troubleshooting.
• Experience in leading programming teams and managing project deliverables.
• Proven ability to work effectively in a cross-functional team environment.

Ideal Candidate:

• Deep expertise in programming for late-phase clinical trials and regulatory submissions.
• Strong communication skills with the ability to collaborate effectively with global teams.
• Demonstrated ability to handle multiple projects simultaneously while maintaining a high standard of work.