
10,000+ employees
Founded 2010
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.
đ April 28
đ California, New Jersey, +1 more states â Remote
đľ $154.3k - $204.3k / year
â° Full Time
đ Senior
đ Director
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10,000+ employees
Founded 2010
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.
⢠Focus on early development (phase I) and late stage (phase II-III) safety science activities ⢠Work closely with the Safety Science group as part of a matrix team ⢠Conduct safety assessment and safety risk management activities based on ICH standards ⢠Provide safety expertise for assigned developmental and/or marketed products ⢠Lead signal evaluation/safety monitoring activities ⢠Contribute and assist in pharmacovigilance activities including benefit/risk regulatory activities ⢠Analyze and author safety assessment reports ⢠Collaborate with PSLs, scientists, pharmacoepidemiologists, and other cross-functional personnel ⢠Lead preparation and presentation of safety data at safety governance meetings
⢠PharmD or PhD in a medical field or biological science and 4+ years of experience in pharmacovigilance in an analytical role ⢠RN with 8+ years in pharmacovigilance in an analytical role ⢠MD or internationally recognized equivalent plus accredited residency or comparable post-medical school clinical training relevant to the country of hiring ⢠4+ years of clinical experience with patients in a relevant therapeutic area specialty ⢠Significant knowledge of general medicine ⢠2+ years of pharmaceutical/biotechnology industry experience in Safety Science, Clinical Development, or Clinical Research is preferred ⢠US trained physicians must have achieved board eligibility or certification
⢠Medical ⢠Dental ⢠Vision ⢠401(k) ⢠FSA/HSA ⢠Life Insurance ⢠Paid Time Off ⢠Wellness
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