Senior Statistical Programmer – Permanent Homebased

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Works in partnership with study teams to create data structures and specifications for ad hoc and study deliverables, including but not limited to ADaM datasets, Tables, Figures, Listings, and Analysis Submission content.

• Collaborates with study teams to guarantee the quality and precision of clinical data, ensuring it is submission-ready in compliance with authority requirements (i.e., SDTM, ADaM, tables, figures, listings, define.xml).

• Takes the lead in managing efforts for pooled and exploratory analyses, working closely with the Statistics TA lead and/or study statisticians, as well as the clinical programming team and their legacy data collection.

• Oversees the in-house specification and delivery of ISS and ISE datasets and related outputs (tables, figures, and listings) when not supplied by the CRO.

• Directs the design and implementation of complex SAS programs for applications intended to analyze and report intricate clinical trial data in CDISC ADaM format.

• Manages the development of global tools aimed at enhancing the efficiency and capacity of the Statistical Programming group.

• Collaborates closely with clinical study teams to plan and execute activities that ensure project timelines are adhered to, delivering high-quality results.

⛳️ Requirements

• Bachelor’s degree in Computer Science, Mathematics, Statistics, or a related field, accompanied by relevant experience.

• A minimum of 5 years of experience in clinical programming and/or statistical programming within the CRO/pharmaceutical sector, utilizing SAS Software.

• Comprehensive understanding of clinical programming and/or statistical programming processes and standards.

• Extensive experience with statistical programming using SAS software, including the development and utilization of SAS Macros.

• Strong programming capabilities and problem-solving skills.

• Proficient in R Programming (trained/hands-on experience).

• Advanced understanding of CDISC standards (CDASH, SDTM, ADaM).

• Documented experience in leading programming activities for pooled and exploratory analyses across multiple clinical studies and submission activities (or equivalent).

• Demonstrated ability to work effectively both independently and as part of a team, achieving set goals while managing personal timelines.

• Experience collaborating within cross-functional, multicultural, and international clinical trial teams.

🏝️ Benefits

• Opportunities for home-based remote work.

• Excellent work/life balance.

• Collaborate on projects and innovations with industry leaders in the Pharma and CRO sectors.

• A cohesive team environment that promotes a collaborative approach to study work.

• Exposure to a variety of therapeutic areas, indications, and study phases.

• Job stability with long-term engagements and development opportunities.

• Potential for career advancement.