(CW) Data Scientist
Company: BioMarin Pharmaceutical Inc.
Location: San Rafael
Posted on: January 10, 2026
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Job Description:
The RBQM Data Scientist supports central monitoring and
risk-based quality management (RBQM) for clinical trials. This role
focuses on implementing and running pre-defined KRIs, QTLs, and
other risk metrics using clinical data, with strong emphasis on SAS
programming to deliver robust and scalable analytics across
multiple studies. KEY RESPONSIBILITIES: The RBQM Data Scientist may
perform a range of the following responsibilities, depending upon
the studies’ complexity and studies’ development stage: • Implement
and maintain pre-defined KRIs, QTLs, and triggers using robust SAS
programs/macros across multiple clinical studies. • Extract,
transform, and integrate data from EDC systems (e.g., RAVE) and
other clinical sources into analysis-ready SAS datasets. • Run
routine and ad-hoc RBQM/central monitoring outputs (tables,
listings, data extracts, dashboard feeds) to support signal
detection and study review. • Perform QC and troubleshooting of SAS
code; ensure outputs are accurate and efficient. • Maintain clear
technical documentation (specifications, validation records, change
logs) for all RBQM programs and processes. • Collaborate with
Central Monitors, Central Statistical Monitors, Data Management,
Biostatistics, and Study Operations to understand requirements and
ensure correct implementation of RBQM metrics. Qualifications
Education & Experience • PhD, MS, or BA/BS in statistics,
biostatistics, computer science, data science, life science, or a
related field. • Relevant clinical development experience
(programming, RBM/RBQM, Data Management), for example: o PhD: 3
years o MS: 5 years o BA/BS: 8 years Technical – Required •
Advanced SAS programming skills (hard requirement) in a clinical
trials environment (Base SAS, Macro, SAS SQL; experience with
large, complex clinical datasets). • Hands-on experience working
with clinical trial data. • Proficiency with Microsoft Word, Excel,
and PowerPoint. Technical – Preferred / Strong Plus • Experience
with RAVE EDC. • Awareness or working knowledge of CDISC, CDASH,
SDTM standards. • Exposure to R, Python, or JavaScript and/or
clinical data visualization tools/platforms. Domain & Soft Skills •
Knowledge of GCP, ICH, FDA guidance related to clinical trials and
risk-based monitoring. • Strong analytical and problem-solving
skills; ability to interpret complex data and risk outputs. •
Effective communication and teamwork skills; comfortable
collaborating with cross-functional, global teams. • Ability to
manage multiple programming tasks and deliver high-quality work in
a fast-paced environment. Note: This description is not intended to
be all-inclusive, or a limitation of the duties of the position. It
is intended to describe the general nature of the job that may
include other duties as assumed or assigned. Equal Opportunity
Employer/Veterans/Disabled An Equal Opportunity Employer. All
qualified applicants will receive consideration for employment
without regard to race, color, religion, sex, sexual orientation,
gender identity, national origin, or protected veteran status and
will not be discriminated against on the basis of disability.
Keywords: BioMarin Pharmaceutical Inc., West Sacramento , (CW) Data Scientist, Science, Research & Development , San Rafael, California
