Senior Statistical Programmer
Job Summary
Job Description
The Senior Statistical Programmer plays a critical role in supporting clinical trial analysis by delivering high-quality, submission-ready datasets and outputs. Working within eClinical Solutions’ technology-driven environment, this role combines advanced SAS programming expertise with leadership responsibilities to ensure accurate, efficient, and compliant statistical deliverables across multiple clinical studies.
Responsibilities:
- Serve as Lead Statistical Programmer for assigned clinical trial projects.
- Develop specifications and SAS programs for SDTM and ADaM datasets.
- Create and validate Tables, Listings, and Figures to support statistical analysis.
- Lead end-to-end programming and quality control activities across multiple studies.
- Develop reusable SAS macros to improve efficiency and standardization.
- Collaborate with biostatisticians and cross-functional teams to meet project timelines.
Requirements:
- Bachelor’s degree or equivalent work experience in a related field.
- 5+ years of experience in pharmaceutical, biotechnology, or clinical research programming.
- Strong expertise in SAS programming, including Base SAS, PROC SQL, macros, and ODS.
- In-depth knowledge of CDISC standards including SDTM and ADaM.
- Experience supporting regulatory submissions and NDA filings.
- Strong understanding of ICH/GCP guidelines and clinical trial methodologies.
Benefits:
- Competitive salary with remote-first work environment.
- Opportunity to work on global clinical trials impacting patient outcomes.
- Award-winning culture recognized for remote work and employee experience.
- Collaborative, inclusive, and growth-oriented workplace.
This role offers the opportunity to advance your career while contributing to innovation in clinical research and healthcare.
