Regeneron is a biotechnology company dedicated to turning scientific discoveries into life-changing medicines. The company focuses on a range of serious diseases including allergic, cardiovascular, and metabolic diseases, neuroscience, oncology, hematology, ophthalmology, and rare diseases. It achieves this by integrating biology and technology to develop cutting-edge biologics and genetic medicines. Regeneron is committed to health equity, environmental sustainability, and supporting future STEM talent through initiatives like the Regeneron Science Talent Search. By maintaining high ethical standards and corporate responsibility, Regeneron aims to push the boundaries of science for better healthcare solutions.
10,000+ employees
Founded 1988
𧬠Biotechnology
π Pharmaceuticals
βοΈ Healthcare Insurance
π° Post-IPO Equity on 2023-10
April 16
πΊπΈ United States β Remote
π΅ $126.7k - $206.9k / year
β° Full Time
π Senior
π΄ Lead
π Manager
π¦ H1B Visa Sponsor
Regeneron is a biotechnology company dedicated to turning scientific discoveries into life-changing medicines. The company focuses on a range of serious diseases including allergic, cardiovascular, and metabolic diseases, neuroscience, oncology, hematology, ophthalmology, and rare diseases. It achieves this by integrating biology and technology to develop cutting-edge biologics and genetic medicines. Regeneron is committed to health equity, environmental sustainability, and supporting future STEM talent through initiatives like the Regeneron Science Talent Search. By maintaining high ethical standards and corporate responsibility, Regeneron aims to push the boundaries of science for better healthcare solutions.
10,000+ employees
Founded 1988
𧬠Biotechnology
π Pharmaceuticals
βοΈ Healthcare Insurance
π° Post-IPO Equity on 2023-10
β’ Lead and support all programming activities per the project strategies within therapeutic area(s). β’ Work with management and study team, plan and own the implementation and execution of programming project standard. β’ Ensure all programming results are delivered in a timely manner with high quality. β’ Coordinate programming documentations and specifications for multiple studies. β’ Act as a technical resource for programming group to provide advice on complex programming tasks. β’ Support global regulatory authority submissions, preparing programming result for submission. β’ Mentor and Coach new hires and junior programmers.
β’ Proficiency in SAS programming skills in a clinical data environment with excellent analytical skills. β’ Knowledge of other programming languages such as R, Python etc. is a plus. β’ Understanding of pharmaceutical clinical development across multiple therapeutic areas and good knowledge of regulatory submissions and requirements β’ Ability to work on global interdisciplinary teams. β’ Good organizational, interpersonal, communication, and leadership skills. β’ Ability to influence others, mentor, and coach junior programmers to achieve results.
β’ health and wellness programs β’ fitness centers β’ equity awards β’ annual bonuses β’ paid time off for eligible employees at all levels
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