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The Associate Director will lead the development of regulatory strategies, manage CMC submissions, and ensure compliance with health authority requirements for small molecules.

The Product Manager will collaborate across teams for market analysis, brand strategy development, promotional campaigns, and relationship management with healthcare professionals to ensure product launch success.

The Senior Regional Clinical Study Manager leads regional clinical operations teams, manages clinical study delivery, timelines, and budgets, ensures compliance, and collaborates with stakeholders to drive trial feasibility and execution.

Sales Representatives work closely with cross-functional teams to manage key accounts, execute sales strategies, gather market intelligence, and meet sales targets.

Support implementation of the Culture of Quality program, enhance Quality communications (webpage, newsletters, sessions), create a Quality department storyboard, produce graphic and digital content, collect and analyze data, and collaborate cross-functionally to advance quality initiatives.

Lead study start-up, maintenance, and closeout activities for clinical trials. Prepare submissions, negotiate contracts, and ensure compliance with regulations. Mentor junior staff and improve processes.

The Marketing and Market Access Manager will develop marketing strategies, drive product launches, and enhance market access for oncology products. Responsibilities include market analysis, stakeholder engagement, and leading pricing strategies. The role requires collaboration with cross-functional teams, understanding healthcare systems, and building patient advocacy plans.

Drive territory sales of BeOne oncology products by developing and executing territory and key account plans, engaging HCPs/KOLs, using data/CRM to prioritise interactions, collaborating cross-functionally, educating clinicians on product data, ensuring compliance, and meeting business targets while travelling within the assigned region.

The Associate Director will drive digital tool adoption, develop communication strategies, train users, monitor progress, and oversee AI capabilities in Quality processes.

Lead global strategic feasibility for clinical studies by integrating internal and external data, advising country/site selection, recruitment and operational strategies, improving feasibility processes and tools, and partnering with program and study teams to optimize study design and execution across early to late-stage programs.