Associate Director, Biostatistics

🔥 15 hours ago

🇺🇸 United States – Remote

💵 $162.6k - $212.6k / year

⏰ Full Time

🟠 Senior

👔 Director

👻 Ghost score 0%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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BeOne Medicines

WebsiteLinkedInAll Job Openings

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.

📋 Description

• Work with cross-functional study/project teams supporting hematology studies • Interact with Clinical, Regulatory, Statistical Programming, Data Management, and other Research Scientists • Review data and develop and implement statistical analysis plans for clinical study reports and health authority submission documents • Provide content for manuscripts and presentations • Provide statistical support in designing and analyzing clinical trials • Coordinate statistical activities for clinical projects • Develop or assist with development of study protocols and statistical analysis plans • Determine appropriate statistical methodology for data analysis • Participate in database design meetings to ensure data quality and analysis requirements • Collaborate with statistical programming staff to ensure programs meet analysis, internal SOP, and regulatory requirements • Analyze clinical trial data and interpret results under supervision • Prepare oral and written reports communicating clinical trial results • Respond to study design, analysis, and interpretation queries from clinical monitors, regulatory agencies, and investigators • Participate in research activities for innovative statistical methods and applications in clinical trial development

🎯 Requirements

• 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 • Experiences with clinical trials required • Knowledge of regulatory guidance required • Knowledge of SAS and/or R is strongly desirable • Oncology experience preferred but not required • Demonstrated written and oral communication skills • Ability to work within a team and work independently • Interdependent/analytic thinking skills • Ability to build strategic working relationships • Good decision-making capability

🏖️ Benefits

• Annual bonus plan eligibility for non-commercial roles • Incentive compensation plan eligibility for commercial roles • Discretionary equity awards • Employee Stock Purchase Plan • Medical insurance • Dental insurance • Vision insurance • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness