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!
Designs, develops, and modifies SAS programs to analyze and evaluate clinical data in accordance with statistical analysis plans. Recognizes inconsistencies and initiates resolution of data problems. May participate in the review of key study and project documents and analysis or data set specifications. Acts as a liaison between clinical, drug safety, and study programming teams as needed. Writes and tests programs of moderate complexity. May write requirements and specifications, understands study- and project-level documentation. Ensures adherence to regulatory and company standards.
- Under minimal supervision, develop and validate SAS® programs to produce high-quality deliverables within set timelines in accordance with company and regulatory requirements. The deliverables include datasets, tables, listings and figures Independently implement routine analysis algorithms for assigned project or study Provide statistical programming support for one or more studies or projects 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 Participate in advisory capacity in initiatives that facilitate standards, infrastructure, and process enhancements across Biometrics
- BS or equivalent relevant education and 4+ years or MS/PhD and 3+ years of SAS® programming experience 2 years of programming experience using SAS® in Pharmaceutical, Biotechnology, Medical Device, or CRO industries Proficiency in SAS® programming Demonstrated proactivity and strong attention to detail Understanding of and hands-on experience with CDISC SDTM and ADaM standards Understanding of drug development process
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.