Principal, Statistical Programming

Principal, Statistical Programming at Edwards Lifesciences in Boise, Idaho, United States Job Description Imagine how your ideas and expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to increase access to pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize patient outcomes. Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. How you'll make an impact: + Develop, test, validate, document, maintain and execute programs in SAS and serve as lead programmer. He/she will take primary role in review and validation of SAS programs created by more junior-level programmers. In addition, will ensure that all appropriate documentation is appropriately filled out and approved. + Provide programming expertise on one or more clinical trials in programming, documentation, validation and review of summary tables, data listings, and graphs for inclusion in clinical reports or presentations in collaboration with project statistician + Lead in programming analysis datasets + Provide programming expertise on ad hoc data requests in collaboration with project statistician + Develop program specifications and design documents in partnership with project statistician. + Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming, reporting, and review + Mentor, coach, and provide guidance to junior-level programmers + Collaborate with CDM to review draft CRFs (Case Report Form), databases and perform edit checks + Partner with clinical data management team to ensure that the databases is defined consistency across clinical trials + Participate in the development of procedures (e.g. SOP development and standardization of output) + Assist in compiling technical documents for internal and external audits; Other duties To view full details and how to apply, please login or create a Job Seeker account