Responsible for start-up activities in Germany and Austria, ensuring timelines and quality standards are met, and providing expertise in clinical trial processes.

The Associate Director is responsible for overseeing clinical operations in Turkey, managing teams, ensuring regulatory compliance, and optimizing trial performance.

The Director of Quality Project Portfolio oversees GxP CI/OE projects, ensuring alignment with quality objectives and business strategy while managing resources and stakeholder communication.

The Study Start-Up Specialist collaborates on study start-up activities, ensures compliance with regulations, manages site performance, and proposes process improvements.

The Associate Director, Quality Excellence leads quality improvement initiatives, mentors teams, and enhances quality management processes in a GxP environment.

The Associate Director, Regional Marketing leads marketing strategies for hematology oncology products, focusing on KOL engagement and collaboration across teams while driving business results.

The Sr. Director will lead the incentive compensation strategy, oversee the US team, ensure compliance, and provide expertise to drive commercial success.

The Senior Manager, Global Solid Tumor Forecasting is responsible for creating and managing commercial forecasts for oncology treatments, utilizing data analytics to inform strategic decisions and collaborating cross-functionally to optimize performance.

The Associate Director of Investor Relations will develop and execute communication strategies, prepare earnings materials, and enhance investor relations processes.

Lead and manage a team of product managers to drive digital transformation, define product vision, and oversee product planning throughout the lifecycle.

The Marketing and Market Access Manager will lead commercialization strategies for the Oncology portfolio, focusing on launch preparations, market access, pricing strategies, and stakeholder engagement. Responsibilities include developing marketing tools, managing affiliate strategies, and enhancing patient advocacy efforts to ensure successful product launches and market positioning.

The Quality Assurance Specialist supports drug manufacture and releases, reviews batch records, collaborates with CMOs, and maintains quality compliance.

This role involves overseeing pharmacovigilance and quality assurance in Serbia, ensuring patient safety, regulatory compliance, and managing local quality systems.

The Director of Quality for the Mexico and LATAM cluster will oversee the affiliate setup and ensure compliance with GMP/GDP standards in the region. They will manage quality agreements, evaluate distributors, and lead quality processes for clinical and commercial products, ensuring regulatory compliance and quality oversight. The role requires collaborations across various departments and participation in audits and inspections.

The Country General Manager will establish BeOne Medicine Ltd in Serbia, drive business operations, manage regulatory affairs, and develop growth strategies in the oncology market.

The IT Financial Analyst manages technology budgets, financial reporting, and contract processing, ensuring effective collaboration with IT and finance teams.

The Senior Manager oversees GCP audits for compliance and conducts audits while ensuring integrity and safety in clinical research. Responsibilities include audit planning, conducting audits, reporting findings, and mentoring junior auditors.

The Logistics Senior Manager oversees the distribution and compliance of biotech products, managing logistics, budgets, and cross-functional collaboration to ensure optimal supply chain operations.

The QMS Process Owner manages Quality Management System processes, ensuring compliance, continuous improvement, and effective training strategies while leading cross-functional collaborations.

The Senior Director leads digital QMS initiatives, ensures regulatory compliance, manages systems, oversees teams, and enhances operations through AI.