Director, Scientific Programming

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BeOne Medicines

WebsiteLinkedInAll Job Openings

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.

📋 Description

• Collaborate with lead project Biostatistician in project strategic planning and provide overall guidance to the programming team in creation, implementation and maintenance of programming development plans for each project accounting for timelines, resources, and quality deliverables for all project work assigned. • Represent the statistical programming team at Study Management Team and Clinical Development meetings to address deliverables and timelines. • Lead or contribute to the development and implementation of programming resource algorithm. • Collaborate with managers, responsible and accountable for project resource planning and tracking. • Interact and communicate with Statisticians, Data Managers, Clinical Operations, Medical Monitors, and other functions to address programming related study deliverables. • Provide managerial support to one or more employees with overall responsibility of leading, training, and mentoring for effective performance. • Write, test and validate product- and study-level macros and utilities. • Provide expert guidance for programming group on complex programming tasks and/or standards. • Oversee the work in support of clinical trials, ad-hoc analysis requests, data validation, etc. in accordance with all relevant statistical regulatory guidance and standards.

🎯 Requirements

• Master’s degree or PhD preferred or equivalent related experience. • Experience 10+ with Bachelor's, 7+ with Master's and 5+ with PhD. • 5+ years of demonstrated leadership experience. • Expert level knowledge and extensive hands-on experience of CDISC standards such as CDASH, SDTM, and ADaM. • Excellent working knowledge of Base SAS, SAS/STAT, SAS Macro language and SAS SQL; SAS/GRAPH a plus. • Experience in development and implementation of statistical programming standards and procedures. • Experience with the drug development process (pre-, early, late and/or observational) in related industries or academic research. • Experience with oncology trials. • Significant level of technical knowledge in statistical programming using SAS.

🏖️ Benefits

• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness