Overview
The Senior Statistical Programmer Consultant will play a pivotal role in delivering high-quality statistical programming solutions for cardiovascular and renal studies within a global clinical research organization. This position involves direct collaboration with clients and cross-functional teams, requiring strong technical skills and the ability to work independently while ensuring project deliverables are met efficiently. The consultant will utilize their expertise in SAS programming and clinical trial processes to contribute to the success of multiple studies.
Responsibilities
- Develop, validate, and maintain SAS programs for clinical study data analysis and reporting.
- Create datasets, tables, listings, and figures according to study requirements.
- Collaborate with Biostatistics, Data Management, and Clinical teams.
- Ensure programming deliverables meet quality standards and project timelines.
- Participate in study planning, review specifications, and support submission activities.
Requirements
- Bachelor’s degree in computer science, statistics, or related scientific discipline, with 5 years of clinical programming experience; or Master's degree with 6 years of experience.
- Strong SAS programming experience within the pharmaceutical or CRO industry.
- Hands-on experience supporting cardiovascular, renal, or metabolism studies.
- Experience in generating and validating SDTM, ADaM, and TLFs.
- Good understanding of CDISC standards and clinical trial processes.
- Ability to manage multiple priorities in a fast-paced environment.
- Strong communication and stakeholder management skills.
- Experience supporting regulatory submissions is preferred.