Senior Manager, Biostatistics

🕒 June 18

🇺🇸 United States – Remote

💵 $155k - $200k / year

⏰ Full Time

🟠 Senior

👔 Manager

👻 Ghost score 31%

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

• Serve as trial statistician on cross-functional teams for study planning, execution, and reporting • Develop individual protocols/statistical analysis plans and determine appropriate statistical methodologies • Participate in database design meetings to ensure high-quality data satisfying analysis requirements • Collaborate with statistical programming staff to ensure programs meet analysis and external requirements • Work with programmers to provide tables, listings, and graphs, including ad hoc validation • Analyze and interpret clinical trial data to meet study protocol objectives • Conduct ad hoc analyses when applicable • Prepare oral and written reports communicating clinical trial results • Provide statistical input during clinical trial planning and conduct with internal departments and external vendors • Make recommendations and resolve technical, quality, and timeline issues • Participate in innovative statistical methodology development arising from project questions • Provide statistical support for strategies optimizing clinical trial design and responses to regulatory agency requests • Identify potential technical and other problems in study design, conduct, and analysis; propose and implement solutions • Serve as statistical representative on cross-functional project teams • Manage vendors to ensure quality deliverables and adherence to requirements and timelines

🎯 Requirements

• PhD or equivalent degree in statistics/biostatistics or related discipline with a minimum of 3+ years relevant work experience • Master’s degree with a minimum of 5+ years relevant work experience • Knowledge of clinical trial design concepts • In-depth knowledge of all phases of the drug development process • Demonstrated skills in planning, analysis, and reporting of clinical trials • Ability to independently apply and implement basic and complex statistical techniques • Ability to work with clinical and regulatory teams, SAS programming, clinical data management, clinical operations, clinical pharmacology, medical writing, and other functions • Ability to manage vendors and ensure quality of deliverables and adherence to requirements and timelines

🏖️ 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 benefits