(CW) Data Scientist (TEMPORARY) jobs in United States
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BioMarin Pharmaceutical Inc. · 1 day ago

(CW) Data Scientist (TEMPORARY)

BioMarin Pharmaceutical Inc. is a global biotechnology company focused on translating genetic discoveries into new medicines. They are seeking a Data Scientist to support central monitoring and risk-based quality management for clinical trials, with a focus on implementing and running key risk indicators and metrics using SAS programming.

BiotechnologyDeveloper PlatformPharmaceutical
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Comp. & Benefits
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H1B Sponsor Likelynote

Responsibilities

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

Qualification

Advanced SAS programmingClinical trial data experienceRAVE EDCCDISC standards knowledgeAnalytical skillsProblem-solving skillsCommunication skillsTeamwork skillsTime management

Required

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: PhD: 3+ years, MS: 5+ years, BA/BS: 8+ years
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
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

Preferred

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

Benefits

Discretionary annual bonus
Discretionary stock-based long-term incentives (eligibility may vary based on role)
Paid time off
Company-sponsored medical, dental, vision, and life insurance plans

Company

BioMarin Pharmaceutical Inc.

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Founded in 1997, BioMarin is a global biotechnology company dedicated to transforming lives through genetic discovery.

H1B Sponsorship

BioMarin Pharmaceutical Inc. has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (34)
2024 (23)
2023 (24)
2022 (26)
2021 (24)
2020 (19)

Funding

Current Stage
Public Company
Total Funding
$585.8M
2020-05-11Post Ipo Debt· $585.8M
1999-07-26IPO

Leadership Team

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Brian Mueller
Chief Financial Officer
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Cristin Hubbard
Chief Commercial Officer
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Company data provided by crunchbase