
10,000+ employees
Founded 2010
đ§Ź Biotechnology
đĽ Healthcare
đ Pharmaceuticals
Biotechnology ⢠Healthcare ⢠Pharmaceuticals
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 the 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.
đ May 29
đşđ¸ United States â Remote
đľ $119.3k - $159.3k / year
â° Full Time
đ´ Lead
đĽđ Medical Writer
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10,000+ employees
Founded 2010
đ§Ź Biotechnology
đĽ Healthcare
đ Pharmaceuticals
Biotechnology ⢠Healthcare ⢠Pharmaceuticals
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 the 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.
⢠Provides expertise to support the development of high-quality clinical and regulatory documents ⢠Manages assigned writing tasks ensuring adherence to regulatory guidelines ⢠Navigates uncertainties to develop and manage timelines of individual and multiple documents ⢠Identifies needs for process/tool optimization and proposes solutions ⢠Leads development of new training programs for junior MWs
⢠An advanced degree (MS/PhD/PharmD/MD) in life science, pharmacy, medical, or health-related science is preferred ⢠Bachelor's with 5+, MS with a minimum of 4+ years of regulatory document writing (or equivalent) experience, or PhD/PharmD/MD with a minimum of 2+ years of regulatory document writing (or equivalent) experience ⢠Technical expertise in Microsoft Word, Adobe Acrobat, and electronic document management systems ⢠Proficiency in Microsoft Outlook, Excel, and PowerPoint
⢠Medical ⢠Dental ⢠Vision ⢠401(k) ⢠FSA/HSA ⢠Life Insurance ⢠Paid Time Off ⢠Wellness
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