Senior Clinical Programmer
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. Summary The Senior
Clinical Programmer role is responsible for performing clinical
programming activities as delegated by the Program or Study Lead.
The Senior Clinical Programmer role is responsible for executing
clinical programming activities for assigned studies. This includes
oversight of database builds, oversight of all clinical programming
for data transfers, data validation, oversight and creation of
system to system integrations and the generation of complete,
correct and consistently fit-for-purpose operational datasets for
data snapshot and data finalization activities.The Senior Clinical
Programmer will be an individual contributor and will not require
any people management. This position will contribute to and make an
impact on project or study team outputs. Responsibilities For an
assigned study, the Senior Clinical Programmer may perform a range
of the following responsibilities, depending upon the program
complexity and program development stage: Data Management Clinical
Programming Deliverable Development and Execution Collaborate with
Data Manager to complete Data Validation Plans/Data Review Plans,
including the definition of edit checks, data listings, and related
analysis to ensure data collected in complete, in conformance with
parameters and plausible. Review Data Transfer Specifications (DTS)
and conduct clinical programming for import of third-party clinical
data and related reconciliations. Conduct the programming and
execution of Level 1 (edit checks by third party developers), Level
2 (clinical data review listings), and Level 3 (statistical data
analysis / reviews) validation. Conduct Peer Review on Clinical
Programming objects, listings, metrics, graphs, and data
visualizations. Prepare operational, raw data for DB lock or
snapshot Export data from EDC and import from external vendor;
execute data quality checks; convert to SAS datasets; check for
patient ID; ensure review and approval by Global Data Science
stakeholders; lock permissions on folders for limited write access.
Subject Matter Expertise Participate in initiatives aimed at
expanding Global Data Science and Data Management capability in a
designated area of expertise, such as ePRO, Artificial Intelligence
(AI), Imaging, Real-World Evidence, etc. by building best practices
in processes, tools, templates, or other guidance for the subject
area. Education & Experience Degree in Statistics, Computer
Science, or Life Sciences. Master’s preferred; Bachelors acceptable
with relevant experience 2 years’ experience with Master’s, or 5
years with Bachelor’s degree Relevant clinical development
experience inclusive of technical and management experience within
and outside of Data Management 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 , Senior Clinical Programmer, Science, Research & Development , San Rafael, California
