958#Principal Statistical Programmer-Oncology remote
Skills
- Expertise in SAS programming and report generation.
- Knowledge of CDISC data standards and FDA regulated environments.
- Experience with Clinical Study Reports and NDA submissions.
- Strong verbal, written, and interpersonal communication skills.
- Ability to manage multiple tasks and meet project deadlines.
Responsibilities
- Participate in CRF design, database review, and data management planning.
- Produce data listings, summary tables, and graphics for clinical data analyses.
- Integrate data across studies within projects and validate programming outputs.
- Coordinate data transfer and programming standards with CROs and vendors.
- Validate analysis datasets and TFLs from external vendors.
- Collaborate with Biometrics teams on clinical trial data analyses.
- Execute ad-hoc requests including manuscripts, posters, and presentations.
Education
- BA/BS in Computer Science, Statistics, Mathematics or related field with minimum 10 years experience.
- OR MA/MS in related field with 8 years experience.
Benefits
- Opportunity to work directly with a single sponsor while leveraging global CRO resources.
- Supportive and quality-focused work culture with continued professional development.
- Diversity and inclusivity emphasized within the company.
- Global network of over 4,000 professionals and 28 years of experience.
Average salary estimate
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