
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.
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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.
• Provide the medical and clinical expertise needed to perform medical review of Individual Case Safety Report (ICSR) • Serve as safety medical expert to evaluate ICSRs for all company products either marketed or in clinical development • Perform regular medical case review for all ICSRs reported from any source including clinical trials, literature, post-marketing studies and post-marketing spontaneous adverse event reports • Review all AEs and SAEs and determine whether the events are accurately reported and captured as what occurred in patient clinically and confirm that events are correctly coded with MedDRA and confirm seriousness criteria • Assess AE and SAE expectedness for each event per Reference Safety Information (RSI) and ensure correct, consistent interpretation and application to ICSRs • Provide overall case assessment and pharmacovigilance comments on ICSRs as needed • Identify important/critical cases with potential safety signals at single case level
• MD, DO or MBBS or other international equivalent • Medical case review experience and prior biopharmaceutical industry experience preferred • Minimum of 2- 4 years Clinical experience, included training required • Minimum of 8-10 years pharmacovigilance experience preferred, including 2-3 years as a Medical Safety Review Physician is preferred; other MD experience in the pharmaceutical industry may be considered • Excellent communication skills (verbal and writing); Clear and confident presentation skills
• Health insurance • Paid time off
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