What are the responsibilities and job description for the Clinical R Programmer position at BioSano Executive Search?
This is an opportunity to step into a high-impact role at the center of clinical development, where your work directly supports regulatory submissions and influences critical decisions that bring therapies to market. As a Senior Statistical Programmer Analyst, you’ll operate as a trusted expert, leading complex programming and analysis efforts, shaping data standards, and partnering closely with cross-functional teams to deliver submission-ready outputs with precision and speed—all in a fully remote environment.
Key Responsibilities
- Lead SAS programming and analysis to generate analysis datasets, tables, listings, and figures
- Develop and maintain R code for clinical reporting and regulatory deliverables
- Perform validation of programs, datasets, and outputs to ensure accuracy and compliance
- Execute data migrations, verifications, and SDTM/ADaM mapping
- Produce SDTM and ADaM datasets and supporting documentation (e.g., define.xml)
- Generate outputs for clinical study reports (CSR), integrated summaries (ISS/ISE), safety updates, and publications
- Collaborate cross-functionally with internal teams and client stakeholders
- Serve as a subject matter expert in areas such as SAS programming, CDISC standards, deliverables, or related domains
Qualifications
- Bachelor’s degree in Computer Science, Statistics, or related field (Master’s preferred)
- 8 years of experience in statistical programming within a pharmaceutical or CRO environment
- Deep expertise in R (Base, Macro, STAT) and clinical data standards (CDISC, SDTM, ADaM)
- Strong understanding of clinical reporting and regulatory submission requirements
- Experience working across platforms (e.g., Windows, UNIX)
- Strong communication and collaboration skills
- Interest or experience in project leadership is a plus
Target compensation is $122,000-$131,000 plus benefits and the flexibility of working remotely.