The Senior Director, Global Forecasting will lead forecasting strategies and model development for oncology products while collaborating with various teams to support organizational decisions and enhance strategic planning.

The Senior Director will lead KOL customer strategies in lung oncology, manage a team, and drive advocacy and marketing initiatives for product launches.

The Senior Safety Scientist oversees safety management in clinical studies, develops safety documentation, and performs risk management and signal detection activities.

The Vice President of Marketing will develop revolutionary strategies for NSCLC therapies, lead marketing initiatives, manage a marketing team, establish partnerships, and effectively engage with internal and external stakeholders to promote product success.

Lead corporate communications strategies to enhance brand visibility, manage media relations, oversee digital content, and drive engagement across key audiences.

The Vice President will lead the European Value, Market Access & Pricing team, formulating market access strategies and ensuring optimal reimbursement for products in development, especially for cancer treatments.

The Regional IT Lead will establish IT operations in Europe, overseeing local implementations, collaborating with global teams, and ensuring compliance with regulatory standards.

Manage end-to-end supply chain operations for clinical-stage oncology, ensuring timely delivery of materials, compliance with regulations, and process improvements.

As a lead statistician, provide statistical leadership and support for clinical studies, collaborate on study design, and ensure compliance with regulatory requirements.

The Director of Analytical Development will lead analytical strategies for drug development, manage project execution, and ensure cross-functional collaboration for regulatory submissions.

The Senior Director, HEOR/RWE develops strategies for health economics and outcomes research related to oncology products, leads evidence generation initiatives, and collaborates with cross-functional teams to present value propositions to stakeholders.

The role requires leading the strategy and management of Workday Learning and Talent systems, optimizing integrations, consulting with HR, and supporting stakeholders.

Lead and oversee quality systems operations, focusing on GxP compliance, document management, training programs, and process improvements in a clinical-stage biopharmaceutical setting.

This role involves oversight and programming support for oncology clinical trials, ensuring quality delivery of statistical analysis, and mentorship.

The Senior Manager, GMP Quality oversees QA in drug development, collaborating with teams on compliance, process validation, and managing quality oversight for products.

The Senior Manager of GMP Quality oversees quality assurance in pharmaceutical development, ensures compliance, and leads process validation efforts across programs.

Lead global strategy and execution of medical congress activities, advisory board operations, and cross-functional collaboration in oncology medical affairs.

Lead cross-functional planning and execution of integrated evidence generation for oncology products, ensuring alignment across medical and commercial functions.

Lead the design and delivery of training programs to ensure effective use of critical information systems across the organization, particularly in the pharmaceutical sector.

The IS Operations Specialist supports IS organization operations, including budget tracking, procurement coordination, contract management, and vendor administration, while aiding project coordination activities.