BeOne Medicines
10,000+ employees
Founded 2010
🧬 Biotechnology
🏥 Healthcare
đź’Š 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.
Associate Director, Safety Scientist
Job not on LinkedIn
đź•’ April 28
🏄 California, New Jersey, +1 more states – Remote
đź’µ $154.3k - $204.3k / year
⏰ Full Time
đźź Senior
đź‘” Director
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BeOne Medicines
10,000+ employees
Founded 2010
🧬 Biotechnology
🏥 Healthcare
đź’Š 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.
đź“‹ Description
• 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
🎯 Requirements
• 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
🏖️ Benefits
• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness
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