Director, GCO Program Lead

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🔥 1 minute ago

🇺🇸 United States – Remote

💵 $171.9k - $231.9k / year

⏰ Full Time

🟠 Senior

👔 Director

👻 Ghost score 0%

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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

• Lead strategic operational planning and clinical operational performance for designated programs • Act as escalation point for study and compound-related issues • Lead gCSMs and provide mentorship, talent development, performance management, and resource management • Partner with program leads and functional representatives to drive disease and asset strategy • Provide clinical operational insight to governance teams and support program strategy • Lead or participate in KOL engagement activities • Evaluate strategic feasibility and budget estimates for new clinical development plans and strategy changes • Allocate resources and initiate CST formation • Create annual program budgets and resource forecasts • Create, review, maintain, and provide input on compound-level documents including IB, DSUR, and protocols • Oversee study planning and execution within the designated program • Conduct program review meetings and track studies against approved budgets and timelines • Report study status, goals, operational KPIs, and quality KPIs • Evaluate preferred global vendors and participate in vendor governance meetings • Provide line management and mentorship to gCSMs • Drive scientific knowledge development and process improvement within Clinical Operations • Collaborate with cross-functional leaders to support clinical development goals

🎯 Requirements

• Bachelor or higher degree in a scientific or healthcare discipline • 10+ years’ experience in the clinical trial industry • Lung cancer experience • Project management exposure/experience across the entire lifecycle of multi-region/country clinical trials in a fast-paced global environment • Experience in people management and program management preferred • Microsoft Office skills • Deep understanding of ICH/GCP Guidelines and other applicable regulatory requirements • Clinical documentation and records management • Clinical operations management • Contract management • Data management • Feasibility studies • Project/program design • Project/program management • Risk management • Technical reporting • Resource management • Travel may be required as per business need

🏖️ 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

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