Principal 1, Statistical Programming Location Brisbane, California Apply
BioMarin is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These conditions are often inherited, difficult to diagnose, progressively debilitating and have few, if any, treatment options. BioMarin will continue to focus on advancing therapies that are the first or best of their kind.
BioMarin's Research & Development group is responsible for everything from research and discovery to post-market clinical development. Research & Development 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 rare diseases. Come join our team and make a meaningful impact on patients' lives.
The Senior Statistical Programmer applies advanced programming techniques and leads the planning, design, development, verification, implementation and maintenance of software used for monitoring, analyzing and reporting of clinical trials data in support of regulatory submissions and publications
Adheres to departmental procedures and practices, technical and industry standards and programming concepts and conventions during all aspects of work
Builds effective working relationships with cross functional groups within BioMetrics, the study team and the company
Negotiates effectively to meet study objectives
Leads development and project management of the statistical deliverables planning and design work
Leads assigned statistical programming team project resources and manages the completion of study statistical programming deliverables to meet project timelines
Monitors contractor programmer project activities and reviews contractor programmer deliverables as necessary
Responsible for every aspect of statistical programming deliverables quality
Conducts program development and verification, identifies bugs and resolves technical problems
Leads the preparation and distribution of reports to the project team members
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
Participates in the development of standard reporting tools or components and system utilities for the statistical programming group
Contributes to developing BioMetrics SOPs
5 years of SAS programming experience in pharmaceutical and/or biotech company
BS in Math, Statistics, Computer Science, Biostatistics, Life Sciences or related applicable field
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.