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Principal Statistical Programmer

Employer
Seagen
Location
Bothell, Washington State
Salary
Competitive pay, 401k, Medical/Dental/Vision benefits
Closing date
Jul 30, 2022
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Job Details

Seagen is a global, multi-product biotechnology company dedicated to developing and commercializing transformative cancer medicines. As the industry leader in antibody-drug conjugate (ADC) technology, we pioneered a new generation in the science of harnessing antibodies to deliver cell-killing agents directly to cancer cells. Seagen’s dedication to improving the lives of cancer patients goes beyond science, and we believe that every employee has a role in contributing to this mission. By working together with a shared dedication and diverse perspectives, we are able to reach our full potential and make a real difference in the world. Seagen is a fast-growing company and has an abundance of opportunities available for you to grow your career. Put your passion to work at Seagen and join us! 

Summary: 

Design, develop, and modify SAS programs to analyze and evaluate clinical data in accordance with statistical analysis plans. In a leadership role on a study, project, or integration, interact with cross-functional teams at a high level to proactively determine programming tasks, timelines, assignments, and resource requirements and oversee study, project, or integration programming efforts to ensure the timely delivery of high-quality output according to company and industry standards.  Represent statistical programming in the review of key study and project documents and data set or reporting specifications. Recognize inconsistencies and initiate resolution of data problems when necessary. Assist programming management with or be the lead on cross-functional process improvement initiatives and resource allocation.  May oversee activities performed by FSP or contract programmers. 
 

Principle Responsibilities: 

  • Ensure accuracy, completeness, quality, and timely delivery of statistical programming deliverables at the study, project, filing, or small product level  Independently implement complex analysis algorithms for assigned projects or studies  Provide technical leadership to study or project team programmers including efficient programming techniques. Decide on implementation of departmental and product-level standards, tools, and processes in assigned studies, projects, or integrations with advice from the lead programmer  Contribute to project- or product-level specifications based on analysis need and ensure compliance with company and industry standards  Review and provide feedback on deliverables from other clinical groups including but not limited to statistical analysis plans; table, listing, and figure shells; data management plans; data transfer plans; and case report forms  Clear and proactive communication with study and project teams to clarify requirements and specifications, update others on assignment status, and convey data irregularities  Initiate, lead, and participate in planned departmental and cross-functional initiatives that facilitate standards, infrastructure, and process enhancements  Manage resources efficiently across multiple projects to maximize synergies  Assist programming management on resource allocation  Train and mentor new and junior programmers 

Qualifications: 

  • 8+ years (BS) or 6+ (MS/PhD) of SAS programming experience in the Biotechnology, Pharmaceutical, Medical Device, and Healthcare industries  6+ years of experience in performing statistical programming using SAS® for creating and testing analysis datasets, tables, listings and figures for Phase I-IV clinical trials  3+ years of experience in overseeing statistical programming projects, including project management of staff working on those projects  3+ years of experience in writing SAS macros  Expert knowledge and understanding of SAS® programming concepts and skills  Demonstrated proactivity and strong attention to detail  Experience in oncology studies; experience with integrations and e-submissions a strong plus  Good understanding of and hands-on experience with CDISC SDTM and ADaM standards 

 

As the leading employer in our industry in the Pacific Northwest, Seagen is proud to offer a competitive total compensation package as well as a comprehensive benefits program designed to support the whole lives of our employees and their families. Benefits include medical, vision and dental coverage, group and supplemental life insurance, 401(k) with company match, tuition reimbursement, relocation assistance and much more. To learn more about Seagen, please visit www.seagen.com.  

Seagen is an equal opportunity employer. All qualified applications will receive consideration for employment without regard to race, age, gender identity, sexual orientation, color, religion, sex, marital status, national origin, protected veteran status, disability status, or any other status protected by federal, state, or local law.  

To prevent the spread of COVID-19, and as an integral part of its public health and safety measures, Seagen requires that all newly-hired employees be fully vaccinated against COVID-19 before commencing employment, subject to reasonable accommodation and other requirements of applicable federal, state, and local law. 

Company

Seagen is a global biotechnology company that develops and commercializes transformative cancer therapies. We’re driven by a singular mission—to make a difference for people impacted by cancer.

As an industry leader in antibody–drug conjugate (ADC) technology, we pioneered the science of harnessing antibodies designed to deliver cell-killing agents to cancer cells. Three of our four approved medicines are built on this technology.

We also focus our research efforts on novel targeted small molecule therapies. In addition, we are leveraging our expertise in empowered antibodies to build a portfolio of proprietary immuno-oncology agents.

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