Sr. Statistical Programmer Analyst (SAS, Macros, Tools Dev) (Office OR Remote)

Key Skills

Biomarker analytics, CDASH, Microsoft DeepSpeed, Python Programming, PyTorch, R Programming, SAS

Job Description

The Senior Statistical Programmer Analyst will be mainly responsible for statistical programming related standard SAS macros and tools development, as well as supporting study deliverables. This position will report into the Head of Statistical Programming and will interact regularly with statistical programming managers and other statistical or clinical programmers. Demonstrated ability to prioritize work and to effectively communicate and collaborate with key stakeholders within Biometrics. This is a unique opportunity to join a small but growing Biometrics team investigating a diverse portfolio of immuno-oncology therapeutics in early development. The ideal candidate will come with years of advanced SAS macro programming experience, solid industry experience working in a regulated global environment while also demonstrating know-how, flexibility, and scientific curiosity useful for establishing internal infrastructure, developing analysis standards, and driving both formal and exploratory work.

Responsibilities

• Develop standard macros and/or tools as well as relevant documentations for statistical and clinical programming needs.
• Implement programming standard templates, macros, tools where appropriate, and follows the departmental coding practices for statistical programs and datasets.
• 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.
• Demonstrated experience with CDASH and CDISC data standards (SDTM, ADaM) as well as health authority reporting requirements.
• Good knowledge of data standards and demonstrated experience in the handling non-CRF data including proven ability to work with diverse data types.
• Performs stakeholder management, negotiating timelines and scope of deliverables (helping to balance team and company needs with speed, rigor, and clarity of message)
• Provides project management to a study or project team deliverables.

Qualifications

• 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
• Minimum 4+ years of biotechnology or pharmaceutical experience, with (immuno-) oncology experience preferred.
• Excellent SAS programming skills including macro development. Experience working with other languages (R) in validated environments strongly preferred.
• In-depth knowledge in the analysis of clinical trial data, including integrated analysis of clinical trial data with other data types (biomarker, PK/PD, real-world, etc.)
• Experience managing delivery of statistical programming projects by CROs.
• Demonstrated ability to rapidly adapt to changing project and strategic requirements.
• Interest in continuing education, particularly in the areas of business knowledge as well as technology trends for producing analyses and visualizations (particularly with an eye towards reproducibility or interactivity).
• Takes a fit-for-purpose mindset to daily work as well as long-term vision.

This role can be based at our Hayward or Brisbane, CA location (preferred) or can be remote based. The anticipated salary range for fully qualified candidates applying for this position is $145,000 - $165,000 USD annually. This salary range is an estimate of what we reasonably expect to pay for this posted position. The actual salary may vary based on various factors including, without limitation, individual education, experience, tenure, skills and abilities, internal equity and alignment with market data. In addition to a competitive market-based salary, Arcus offers the opportunity to participate in stock programs, a performance-based bonus, and a comprehensive benefits package. Additional information about our total rewards program can be found here: https://arcusbio.com/careers. EOE

Arcus Biosciences is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. Arcus is committed to the principle of equal employment opportunity for all employees and does not discriminate based on race, religion, color, sex, gender identify, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other legally protected status. EOE/AA/Vets