Note: The job is a remote job and is open to candidates in USA. Arcus Biosciences is a growing company focused on immuno-oncology therapeutics. The Senior Statistical Programmer Analyst Contractor will support submission readiness of study data packages and collaborate with various stakeholders in the clinical trial process.
Responsibilities
- Develop specifications, build and execute programs for internal data reviews, publications, exploratory, post-hoc and regulatory review
- Adopts strategic approach to producing and prioritizing analytical deliverables which includes study level or integrated analysis for safety signal detection or other business needs
- Work with data management to review case report forms, database specifications, and data transfer specifications
- Manage on-time and quality delivery of CRO-generated analyses results
- Solid, demonstrated experience with CDASH and CDISC data standards (SDTM, ADaM) as well as health authority reporting requirements
- In-depth knowledge of data standards and demonstrated experience in the handling non-CRF data including proven ability to work with diverse data types
- Responsible for creating/reviewing SDTM/ADaM mapping specifications
- Generates or validates SDTM domains, ADaM datasets, reviewer's guide, and define.xml files
- Generates or validates TFLs to support the statistical analysis of data for clinical studies, regulatory submissions, and publications such as CSR, DSUR, IB, publications, etc
Skills
- Bachelor's or Master's degree in a data science field, e.g., statistics, mathematics, epidemiology, computer science, bioinformatics, or another field with commensurate levels of experience
- 8+ years programming experience with growing responsibility in biotechnology or pharmaceutical clinical trial environment
- Experience in software development and testing (e.g., SAS Macros tools, R functions/packages, Unix scripts etc)
- Experts in developing applications using various technical stacks not limited to SAS, R and/or Python
- Solid understanding of industry standards such as CDISC, specifically SDTM and controlled terminology and/or ADaM
- Proven ability to translate sophisticated problems into clear and concise programming code/tools
- Basic Project management skills and experience
- Solid understanding of programming practices (including tools and processes), relevant health authority guidelines, such as (e.g., ICH‐GCP, 21 CFR Part 11), and relevant clinical R&D concepts
- Demonstrated strong written, verbal communication skills, ability to manage conflicting demands and priorities and to negotiate successfully
Company Overview
Company H1B Sponsorship