Overview
The Senior Statistical Programmer Consultant will work directly with a client while being supported by a global Contract Research Organization (CRO). This role requires a strong focus on programming technical tasks and the ability to collaborate effectively with various stakeholders, ensuring the high quality of programming deliverables in clinical studies within the cardiovascular and renal domains.
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 disciplines with 5 years of relevant clinical programming experience; or a Master’s degree with 6 years of experience.
- Strong SAS programming experience within the pharmaceutical or CRO industry.
- Hands-on experience supporting cardiovascular, renal, and metabolism (CVRM) studies.
- Experience in generating and validating SDTM, ADaM, and TLFs.
- Good understanding of CDISC standards and clinical trial processes.
- Ability to work independently and manage multiple priorities in a fast-paced environment.
- Experience supporting regulatory submissions is preferred.
- Strong communication and stakeholder management skills.