Associate Director, Data Disclosure, Transparency

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BeOne Medicines

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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.

📋 Description

• Supervises BeOne’s Clinical Data Publication activities in accordance with BeiGene policy and international regulations. • Monitors transparency compliance across BeOne’s portfolio of studies. • Write, submit, and manage disclosure and transparency activities. • Supports the development and maintains strategies for improving departmental systems and processes. • Supervises the execution of clinical trial disclosure information to regulatory authorities and Clinical Data Publication submissions. • Ensures up-to-date data disclosure tracking tools and dashboards maintained by team members in compliance. • Directs the development and implementation of special projects and training material for Data Disclosure & Transparency activities. • Represents function at the highest degree with proactive interactions with colleagues. • Provides tactical guidance to department colleagues on global transparency requirements. • Serves as primary point of contact for escalation and resolution of clinical trial transparency issues. • Manages resource planning and deployment to ensure appropriate study/program support.

🎯 Requirements

• 8+ years of relevant experience and a BA or BS or 6+ years with Master or above • Preferably 8 or more years of direct experience in Data Disclosure & Transparency Management • Core understanding and familiarity with clinical development, clinical trial conduct, regulatory submission process, and data disclosure and transparency processes required • Excellent verbal and written skills • Ability to translate complex information into understandable language for diverse stakeholders preferred • Attention to detail, time management, and ability to balance multiple tasks to achieve goals and meet deadlines • Strategic thinking, with a focus on process development, improvement and optimization • Experience with unique problem-solving where issues are not clearly defined and sufficient information to describe problems may not be available

🏖️ Benefits

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