We are seeking a highly skilled Senior Statistical Programmer. This is a lead role and will be responsible for the end-to-end programming and validation of clinical trial datasets, tables, listings, and figures in compliance with regulatory standards. The ideal candidate will have extensive experience supporting oncology clinical trials (Phases I–III).
About the Role
This is a lead role and will be responsible for the end-to-end programming and validation of clinical trial datasets, tables, listings, and figures in compliance with regulatory standards.
Responsibilities
- End-to-end programming and validation of clinical trial datasets.
- Creation of tables, listings, and figures in compliance with regulatory standards.
Qualifications
- 8-10 years of statistical programming experience in the pharmaceutical/biotech/CRO industry.
- Experience with regulatory submissions.
- Oncology
Required Skills
- Efficacy Programming Lead and client facing experience preferred.
- Strong knowledge of CDISC SDTM and ADaM.
Preferred Skills
- Excellent problem-solving skills, attention to detail, and ability to manage multiple priorities.
- Strong communication skills and ability to work in a collaborative, fast-paced environment.