Associate Director, Data Analytics Science
Company: BioMarin Pharmaceutical Inc.
Location: San Rafael
Posted on: October 28, 2025
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Job Description:
Who We Are BioMarin is a global biotechnology company that
relentlessly pursues bold science to translate genetic discoveries
into new medicines that advance the future of human health. Since
our founding in 1997, we have applied our scientific expertise in
understanding the underlying causes of genetic conditions to create
transformative medicines, using a number of treatment modalities.
Using our unparalleled expertise in genetics and molecular biology,
we develop medicines for patients with significant unmet medical
need. We enlist the best of the best – people with the right
technical expertise and a relentless drive to solve real problems –
and create an environment that empowers our teams to pursue bold,
innovative science. With this distinctive approach to drug
discovery, we’ve produced a diverse pipeline of commercial,
clinical and preclinical candidates that have well-understood
biology and provide an opportunity to be first-to-market or offer a
substantial benefit over existing therapeutic options. About
Worldwide Research and Development From research and discovery to
post-market clinical development, our WWRD engine involves all
bench and clinical research and the associated groups that support
those endeavors. Our teams work on developing first-in-class and
best-in-class therapeutics that provide meaningful advances to
patients who live with genetic diseases. The Data Analytics Science
team is responsible for providing statistical application
development leadership, oversight for data standards, and
programming analysis across all molecules. The team is responsible
for leading Data Analytics Science execution for all phases of
clinical trials and drug development, including regulatory
submissions. The Data Analytics Science sub-function develops
validated statistical programs for generating analysis datasets and
evidence reports (TLGs) and implements and utilizes statistical
models to analyze and solve scientific problems in support of
submission and new drug development. About the Opportunity:The
Associate Director will provide statistical programming leadership
and oversight for clinical trials, including regulatory
submissions, and statistical application development. This
individual is also responsible for production of statistical
programming deliverables, either personally, or by directing and
coordinating activities of others, or by supervising programming
managers, programmers, and partnering with vendors and third
parties as applicable. Responsibilities include: · Lead project
programming team to develop datasets (ADaM) and TLGs for clinical
study reports, submissions (NDA/BLA) to worldwide regulatory
agencies (e.g., FDA, EMA), publications, ad hoc and other
statistical analysis requests; carry out integrated analysis if
assigned. Builds effective working relationships with cross
functional groups within Data Science and across BioMarin to ensure
that customer/stakeholder needs are met · Ensure processes and
procedures are carried out in a compliant and consistent manner
according to published guidelines for all assigned compounds.
Effectively utilizes assigned resources as necessary and manages
deliverables completion to meet project timelines · Manage CRO and
FSP programmers study activities and review programming related
deliverables· Conduct program development and verification,
identify bugs, and resolve technical problems· Identify new tools
to increase efficiency and quality Adheres to and responsible for
monitoring compliance with departmental procedures and practices,
technical and industry standards and programming concepts and
conventions during all aspects of work Investigates trends,
identifies techniques and makes recommendations for new methods and
technologies used in pharmaceutical and/or biotech industries for
reporting and managing clinical data Leadership Responsibility:
Provide leadership for departmental strategic initiatives and
process improvement. Guide career growth and provide development
opportunities for analysts and programmers. Monitor project
progress and ensure proper resource allocation for successful
project deliverables against goals and timelines. Managing and
reviewing contractors’ deliverables as necessary Must have: Minimum
Requirements: Master’s degree (preferred) or BA/BS degree with a
focus on computer science, statistics, biostatistics, mathematics,
or other related scientific discipline. 12 or more years of
clinical trial experience, statistical programming, and/or drug
development experience with BA/BS; 10 years with Master’s. Good
knowledge of CDISC standards and programming in SAS Experience with
Regulatory submissions Managing others including managers of
statistical programmers Nice to have: Master’s degree in computer
science, statistics, biostatistics, mathematics, or other related
scientific discipline Experience with programming in R or Python
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., San Rafael , Associate Director, Data Analytics Science, Science, Research & Development , San Rafael, California
