
10,000+ employees
Founded 2010
🧬 Biotechnology
🏥 Healthcare
💊 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.
🕒 July 16
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10,000+ employees
Founded 2010
🧬 Biotechnology
🏥 Healthcare
💊 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.
• Work with cross-functional study/project teams supporting hematology studies • Develop and implement the statistical analysis plan (SAP) for the clinical study report (CSR) • Analyze data and interpret results from clinical trials to meet objectives of the study protocol • Prepare oral and written reports to effectively communicate results of clinical trials • Provide responses to queries relating to study design, analysis, and interpretation posed by clinical monitors, regulatory agencies, and/or investigators • Involved in research activities for innovative statistical methods
• A minimum of a PhD in Statistics or related field with 5+ years of experience, or a Master’s degree with a minimum of 8 years of experience in clinical drug development • Knowledge of SAS and/or R • Experiences with clinical trials and knowledge of regulatory guidance are required • Oncology experience is preferred but not required • Demonstrated written and oral communication skills • Ability to work within a team and work independently
• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness
Apply Now🕒 July 16
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