
BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.
10,000+ employees
Founded 2010
July 17
đşđ¸ United States â Remote
đľ $171.3k - $231.3k / year
â° Full Time
đ Senior
đ Compliance

BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.
10,000+ employees
Founded 2010
⢠Responsible for developing, implementing, and advising on global regulatory strategies ⢠Manage regulatory aspects of compounds through all phases of development ⢠Provide leadership and strategic regulatory oversight for designated projects ⢠Interface with business partners regarding global development and registration strategies ⢠Support the preparation and submission of global regulatory documentation ⢠Maintain awareness of global regulatory environment ⢠Facilitate policy and development of standard interpretation of global regulation ⢠Manage and lead an effective global regulatory project team ⢠Mentor regulatory professionals and help create a goal oriented culture
⢠BS with 10+ years, MS with 7+ years or PhD/MD/PharmD with 5+ years of experience in the biotechnical or pharmaceutical industry ⢠5+ years of experience in a Regulatory capacity with broad and in-depth regulatory knowledge ⢠Experience working as a lead in Regulatory Affairs across two or more major geographic areas ⢠Prior experience with both small molecules and biologics ⢠Sufficient regulatory knowledge to integrate inputs from other countries/regions ⢠Thorough understanding of drug development process and the pharmaceutical industry ⢠Understands scientific and clinical data sufficiently to ask questions and make suggestions ⢠Regulatory experience with INDs/CTAs, NDAs/BLAs/MAAs, lifecycle management
⢠Medical ⢠Dental ⢠Vision ⢠401(k) ⢠FSA/HSA ⢠Life Insurance ⢠Paid Time Off ⢠Wellness
Apply NowJuly 16
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