The Associate Director, HRBP will serve as a strategic partner to U.S. Field commercial leaders, translating business priorities into actionable organizational and talent strategies. They will lead initiatives in workforce planning, organizational design, and leadership development to support the company's growth and operational effectiveness.
The Medical Science Liaison will engage in peer-to-peer scientific dialogue with healthcare professionals and serve as a therapeutic expert to internal teams. They are responsible for cultivating relationships with key opinion leaders and supporting medical strategy across clinical development and commercial functions.
The Director develops and executes global value, access, and pricing strategies for NSCLC assets to ensure sustainable patient access. They lead cross-functional teams to align clinical development, evidence generation, and launch plans with payer and HTA requirements.
Build and lead a national oncology sales organization, including hiring and developing field leaders and teams, setting sales strategy, and delivering successful product launches and revenue targets. Oversee sales operations and strategic account engagement while partnering across commercial, medical, access, and training functions to optimize execution and ensure compliant field activities.
The Associate Director will lead the global digital experience strategy for Medical Information platforms and websites while providing operational support across the product lifecycle. This role involves managing congress booth execution, analyzing inquiry data to inform strategy, and ensuring all scientific content is accurate and compliant.
The Associate Director will develop and maintain scientific response content while ensuring accuracy and compliance with regulatory standards. They will also monitor inquiry trends and provide scientific support for medical affairs initiatives and product launches.
The Director will lead the global strategy, standardization, and continuous enhancement of Medical Science Liaison capabilities across regions. They will design frameworks, tools, and training programs to ensure high-impact scientific engagement and operational excellence.
The Director will lead the development of global Medical Affairs content and training roadmaps to support product launches and scientific fluency. They will collaborate with cross-functional teams to ensure scientific materials are aligned with company strategy and regulatory requirements.
The Executive Director will lead the real-world analytics and programming strategy to generate decision-ready evidence across the product lifecycle. They will build and manage a high-performing team while collaborating cross-functionally to support clinical development, regulatory submissions, and commercialization milestones.
The Medical Science Liaison will cultivate relationships with key opinion leaders and healthcare professionals to facilitate scientific dialogue and provide medical expertise. They will also support clinical trial activities and collaborate cross-functionally to execute medical strategies within their assigned territory.
The lead statistical programmer will manage programming activities for real-world analytics studies from initiation through final delivery. They will collaborate with cross-functional teams to translate study protocols and statistical analysis plans into reproducible programming solutions.
The Medical Science Liaison will execute field medical plans and engage in peer-to-peer scientific dialogue with healthcare professionals to gather meaningful insights. They will also serve as a therapeutic expert and liaison between the company and clinical study sites to support medical education and congresses.
The Director of Global Compensation will design and implement scalable global compensation programs, including base salary, incentives, and job architecture. They will also partner with HR and business leaders to ensure compensation strategies align with organizational goals and regulatory requirements.
The Senior Manager will execute field medical plans in Germany, engaging in peer-to-peer scientific exchange with healthcare professionals and key opinion leaders. They will also collect medical insights, support clinical study site engagement, and contribute to medical education and congress activities.
The Contract Manager will serve as an enterprise-wide contracting partner, drafting, reviewing, and negotiating a high volume of commercial and clinical agreements. They will also manage the end-to-end contract lifecycle and partner with cross-functional stakeholders to ensure compliance and operational efficiency.
The Associate Director is responsible for defining and executing market access strategies to ensure patient access to innovative oncology therapies in Germany. This includes leading value dossier submissions, managing pricing negotiations, and engaging with key external stakeholders and HTA bodies.
The Associate Director will oversee end-to-end distribution operations, managing relationships with 3PLs, specialty distributors, and specialty pharmacies. They will also collaborate with cross-functional teams to ensure operational excellence, compliance, and the successful commercialization of the company's oncology portfolio.
Lead project management support for global commercialization teams to drive alignment, accountability, and execution across strategic priorities. Coordinate inputs across various departments including medical, market access, and regulatory to ensure cohesive commercialization plans.
The Executive Director will lead global collaboration to develop and execute PDAC marketing strategies for lead RAS programs in preparation for product launches. They will partner with cross-functional teams to shape strategic plans, manage promotional tactics, and ensure alignment across clinical, medical, and commercial functions.
The Senior Director will establish global pricing architecture, governance processes, and financial models to support the launch of oncology therapies. They will partner with cross-functional teams to ensure compliant, value-based pricing execution and sustainable patient access across global markets.
The Commercial Lead for Switzerland is responsible for defining and executing the local commercial strategy, including product launches and portfolio growth. They will lead the country commercial organization, manage cross-functional alignment with Medical Affairs and Market Access, and oversee stakeholder engagement.
The Vice President of PDAC Marketing will lead the development and execution of strategic brand plans and launch trajectories for lead RAS programs. This role involves building and managing a marketing team, collaborating with cross-functional partners, and establishing strategic partnerships to drive product growth.
The Medical Science Liaison will execute field medical plans, engage in peer-to-peer scientific exchange with healthcare professionals, and gather medical insights within the Swiss territory. They will also support clinical study site engagement and collaborate cross-functionally to support medical strategies.
The Director of Market Access for BeLux is responsible for defining and executing country-level market access strategies to ensure patient access to innovative oncology therapies. This role involves leading reimbursement negotiations, developing value dossiers, and engaging with key external stakeholders including payers and HTA bodies.
The Associate Director will develop and execute government affairs strategies in Germany to establish the company as a credible partner within the healthcare policy landscape. They will cultivate relationships with government entities and industry stakeholders while providing strategic counsel to leadership.
The Tax Manager will oversee global tax compliance, reporting, and international tax matters, including VAT/GST and transfer pricing. They will also manage domestic tax provisions, SEC disclosures, and coordinate with internal and external teams on audits and tax filings.
The Medical Science Liaison will cultivate relationships with key opinion leaders and healthcare professionals to facilitate scientific exchange and provide medical expertise. They will also collaborate cross-functionally to support clinical development, medical strategy, and the dissemination of scientific data.
The Associate Director will lead national Medical Affairs activities in Germany, establishing scientific relationships with key opinion leaders and healthcare professionals. They will provide medical oversight for cross-functional teams and contribute to clinical research, market access strategies, and the development of medical materials.
The Associate Director will define and execute market access strategies to ensure patient access to innovative oncology therapies in Germany. This includes leading HTA filings, managing pricing negotiations, and engaging with key external stakeholders and health authorities.
The Executive Director will partner with the U.S. General Manager to drive operational excellence, scale organizational capabilities, and ensure cross-functional alignment across the U.S. commercial region. This role involves leading key business processes, managing governance structures, and fostering a unified culture to support the company's oncology portfolio.
The Director will lead the strategy, design, and implementation of global named patient access initiatives for investigational therapies. They will manage cross-functional operations and ensure compliance with regulatory requirements while overseeing vendor partnerships.
The Director will serve as a strategic partner to the VP of US Market Access, driving operational excellence and cross-functional alignment across the organization. They are responsible for translating strategic objectives into actionable plans, managing key business initiatives, and ensuring successful product launches.
The Director will develop and lead strategic net pricing and contracting recommendations to optimize market position and financial outcomes. They will oversee provider contracting strategies and deliver executive-level pricing materials to inform senior leadership decision-making.
The Director, Global Insights will develop and execute a global insights roadmap to inform product strategy and portfolio decisions across the oncology pipeline. They will translate complex market research into actionable strategic recommendations for senior leadership and cross-functional stakeholders.
The Senior Director will lead the development and execution of patient-reported outcomes (PRO) strategies to support clinical development, regulatory submissions, and market access. They will collaborate with cross-functional teams to integrate patient-centered endpoints into study designs and ensure high-quality evidence generation throughout the product lifecycle.
The Senior Director will develop and execute US Medical Affairs strategies, focusing on launch readiness and life cycle management for gastrointestinal and oncology assets. They will serve as a therapeutic area expert, leading cross-functional teams and engaging with key external stakeholders to drive scientific strategy.
The Senior Manager, Patient Access Advocate will act as a single point of contact to manage patient cases, ensuring access to therapies by navigating insurance, benefits, and financial barriers. They will collaborate with healthcare providers, specialty pharmacies, and internal teams to resolve access issues and support the patient journey from enrollment to treatment.
The Senior Manager, Patient Access Advocate will act as a single point of contact to manage patient cases, ensuring access to therapies by navigating insurance policies, benefits verification, and appeals. They will collaborate with healthcare providers, specialty pharmacies, and internal teams to resolve access barriers and support patients throughout their treatment journey.
The Nurse Case Manager will act as a single point of contact to manage patient access, insurance coverage, and financial barriers for oncology therapies. They will collaborate with healthcare providers, specialty pharmacies, and internal teams to ensure seamless patient support and resolve access bottlenecks.
The preclinical study manager oversees operational activities for non-GLP and GLP toxicology studies, serving as the primary liaison between the company and contract research organizations. They ensure scientific objectives are met, manage study timelines, and facilitate regulatory compliance throughout the drug development process.
The Director will lead the development and execution of marketing strategies for pancreatic cancer programs, including launch readiness and in-line business support. They will collaborate with cross-functional teams and manage external agencies to drive brand performance and customer engagement.
The Director, Global Benefits will lead the evaluation, design, and strategic oversight of global benefits programs while building scalable governance and operational frameworks. They will partner with cross-functional teams to ensure competitive, sustainable, and compliant benefits that support a rapidly growing global workforce.
The Associate Director will oversee end-to-end distribution operations, managing relationships with 3PL providers, specialty distributors, and pharmacies to ensure commercial success. They will also collaborate with cross-functional teams to drive process improvements and ensure compliance with regulatory and legal requirements.
The Senior QA Manager will lead internal and external GxP audits, manage supplier quality programs, and ensure compliance with regulatory standards. They will also negotiate quality agreements, monitor supplier performance metrics, and support preparation for regulatory inspections.
The Director of Marketing will lead the development and execution of strategic and promotional plans for RAS(ON) programs in preparation for lung cancer product launches. This role involves collaborating with cross-functional teams, managing agency relationships, and leveraging market insights to drive brand performance.
The Director of Medical Affairs for BeLux is responsible for defining and executing the local medical strategy and leading the medical team for the oncology portfolio. This role involves building strong relationships with key opinion leaders and ensuring scientific excellence while collaborating with cross-functional teams to support product launches and market access.
The Market Access Director is responsible for defining and executing the country market access strategy to ensure timely patient access to innovative oncology therapies in Poland. This role involves leading pricing negotiations, developing value dossiers, and engaging with key stakeholders including payers and HTA authorities.
The Director of Medical Affairs for Poland is responsible for defining and executing the local medical strategy for the oncology portfolio. This role involves leading scientific exchange, building relationships with key opinion leaders, and ensuring alignment between global strategy and local healthcare needs.
The Medical Science Liaison will engage in peer-to-peer scientific dialogue with healthcare professionals and serve as a key liaison between the company and clinical study sites. They will also provide scientific support for medical congresses, advisory boards, and internal teams to advance medical strategies.
The Senior Director will lead the development and execution of oncology-focused Corporate Affairs strategies in Italy, encompassing media relations, public affairs, and internal communications. This role involves building executive visibility, managing corporate reputation, and ensuring alignment with regional and global company objectives.
The Senior Manager will lead the scaling of global inventory and cost accounting processes, including standard costing and ERP system development. They will also partner with cross-functional teams to manage inventory valuation, transfer pricing, and audit compliance.
The Medical Science Liaison will execute field medical plans, engage in peer-to-peer scientific exchange with healthcare professionals, and gather medical insights within the UK territory. They will also support clinical study site engagement and collaborate cross-functionally with internal teams to advance the company's oncology pipeline.
The MSL will execute field medical plans in France by engaging in scientific dialogue with healthcare professionals and cultivating relationships with Key Opinion Leaders. They will serve as a therapeutic expert and liaison between the company and clinical study sites to support medical education and congresses.
Lead the drafting and management of complex clinical regulatory documents such as protocols, CSRs, and NDA modules. Act as the primary medical writing contact for clinical development programs and mentor junior writers.
This role focuses on improving the adoption of Digital and AI capabilities by creating a governed system for knowledge capture and training content management. It involves managing the AI Champion Network and translating technical outputs into reusable enterprise assets.
Lead and develop a team of Senior Oncology Account Managers to exceed performance targets in the North-Center area of Spain. Drive commercial success by implementing sales strategies and managing key relationships with healthcare accounts and regional stakeholders.
Lead the global commercial precision medicine and companion diagnostics strategy to ensure successful product launches and maximize patient access. Partner with cross-functional teams and external diagnostic partners to integrate biomarker strategies into therapeutic development and commercialization.
The MSL will engage in peer-to-peer scientific dialogue with healthcare professionals and KOLs to gather insights and advance medical knowledge. They will serve as a therapeutic expert and liaison between the company and clinical study sites, supporting medical congresses and advisory boards.
The Senior Oncology Account Manager is responsible for promoting oncology products and building professional relationships with healthcare providers and stakeholders in Germany. The role involves strategic territory management, implementing integrated initiatives to achieve sales goals, and collaborating cross-functionally to improve patient access to care.
Define and drive global value, access, and pricing strategies for oncology assets across their entire lifecycle. Influence clinical development and evidence generation to maximize long-term asset value and ensure sustainable patient access.
Develop and execute HEOR/RWE strategies to demonstrate the value of oncology products for pancreatic and colorectal cancers. Collaborate with cross-functional teams to optimize Integrated Evidence Plans and engage with external payers and HTA agencies.
Lead and develop a team of 8 sales representatives to exceed performance targets for oncology products in the Northeast region. Manage strategic relationships with major health systems and GPOs while collaborating with cross-functional partners to drive product utilization.
Lead engagement with Lung Cancer Key Opinion Leaders in the Central Rockies to inform brand strategy and execute commercial tactics. Collaborate cross-functionally to support the US launch of RAS(ON) inhibitors and communicate market insights to the organization.
The Director will develop and execute regional CMC regulatory strategies to support clinical development, marketing authorizations, and lifecycle management in Europe. They will serve as the primary lead for interactions with the EMA and national competent authorities while providing strategic guidance across cross-functional teams.
