The Study Start-Up Specialist supports the delivery of study start-up activities, including site selection, activation, and regulatory submissions. They are responsible for maintaining high-quality documentation, managing site relationships, and ensuring compliance with ICH/GCP and internal SOPs.
The Key Account Manager will promote oncology products to healthcare professionals and stakeholders while driving commercial negotiations. They are responsible for developing territory plans, managing customer relationships, and achieving specific sales objectives.
The Clinical Research Associate II is responsible for conducting site visits, monitoring data quality, and ensuring patient safety in accordance with ICH-GCP guidelines. They also manage site relationships, provide protocol training, and oversee site performance metrics to ensure study milestones are met.
The Global Clinical Study Manager is responsible for the end-to-end delivery of global oncology clinical studies within budget and timeline constraints. They lead cross-functional teams, manage external vendors, and ensure inspection readiness and regulatory compliance throughout the study lifecycle.
The Global Clinical Study Manager is responsible for the end-to-end delivery of global clinical studies within budget and timeline constraints while ensuring inspection readiness. They lead cross-functional teams, manage external vendors, and oversee all operational aspects from feasibility to study closeout.
Lead global clinical studies from feasibility through closeout, coordinating cross-functional teams and external partners to deliver within agreed timelines, budgets, and quality standards. Oversee study planning, risk and quality management, regulatory readiness, vendor and resource management, and continuous process improvement.
The Contract Manager oversees the administration, drafting, and negotiation of clinical site contracts to ensure compliance with legal, regulatory, and Fair Market Value standards. They also provide study-level guidance, mentor team members, and serve as a primary point of contact for clinical operations and legal teams.
Oversee regulatory review and provide strategic guidance for promotional and non-promotional communications and product labeling, ensuring compliance with applicable requirements and approved labeling. Lead cross-functional regulatory work, advise and train business teams, engage with regulatory authorities as needed, and develop and mentor regulatory professionals.
Design and govern scalable R&D data models, ontologies, schemas, and integration standards, ensuring performance, interoperability, and compliance with FAIR and GxP requirements. Lead model delivery and architecture consulting, partner with business and technical stakeholders, and mentor colleagues while supporting data warehouse and cloud data lake implementations.
Lead the strategy, development, and launch of integrated customer engagement experiences across the hematology portfolio, including digital campaigns and CRM journeys. Drive cross-functional execution by partnering with internal stakeholders and external agencies to ensure compliant and effective market-facing solutions.
The R&D Data Steward II supports the implementation and maintenance of data governance standards to ensure R&D data assets are accurate and well-documented. This role involves executing data quality checks, managing metadata, and collaborating with cross-functional teams to uphold compliance and data integrity.
Manage commercial labeling artwork from initiation through approval, production implementation, and lifecycle updates for product packaging, including inserts, cartons, and containers. Coordinate cross-functional teams and external partners, maintain change-control and quality records, and improve processes to deliver accurate artwork on schedule for regulatory submissions and product launches.
The Senior Manager will oversee global contract manufacturing partnerships, driving productivity and ensuring quality, cost, and performance goals are met. They will also lead cross-functional project teams to manage new product introductions and market launches while maintaining supply chain stability.
The Clinical Research Associate II is responsible for conducting site visits, ensuring protocol and regulatory compliance, and maintaining effective relationships with investigative sites. They also monitor data quality, provide site training, and mentor less experienced staff to ensure study milestones are met.
The lead is responsible for identifying systemic compliance issues and trends across the EMEA region to drive continuous improvement in clinical trial execution. They will partner with global teams to integrate risk management strategies and facilitate the implementation of process enhancements.
The Key Account Manager will develop and execute national plans to drive stakeholder engagement and ensure access to innovative oncology treatments. They are responsible for achieving sales targets, managing regional budgets, and collaborating with healthcare practitioners and payers to optimize patient care.
The Director will lead the development and implementation of global commercial strategies and launch roadmaps for the sonrotoclax brand. This role involves coordinating with cross-functional partners and local markets to ensure integrated launch planning and effective execution of core commercial content.
The Director provides global strategic leadership for contamination control and microbiology governance across manufacturing sites to ensure product safety and regulatory compliance. They lead complex microbial investigations, drive harmonization of practices, and provide technical expertise for new technology implementations and facility modifications.
The Key Account Manager will manage strategic accounts and develop the territory within the public hematology market, focusing on patient journeys and sustainable access to treatments. They will map decision-makers, execute account plans, and drive scientific sales while ensuring compliance with public sector regulations.
The Sr Manager of Clinical Supply Chain oversees drug supply activities, including planning, labeling, and distribution for clinical studies. They represent the supply chain on clinical study teams and manage relationships with external CMOs and vendors to ensure continuous supply.
The Key Account Manager will lead strategic account management and territory development within the private hematology market. They are responsible for driving scientific demand, managing institutional access, and achieving sales targets through collaborative stakeholder engagement.
The Associate Director will lead the cross-functional planning and execution of global solid tumor medical initiatives and drive the development of integrated evidence plans. They will also facilitate alignment across disease teams and franchise leadership while implementing process improvements to enhance operational efficiency within the PMO.
The Business Unit Director will lead the commercial strategy and execution for the Solid Tumor portfolio in Israel, overseeing the entire product lifecycle from pre-launch to growth. This role involves managing cross-functional teams, driving business performance, and ensuring alignment with regional and global portfolio strategies.
The GCO Program Lead is responsible for the strategic operational planning and clinical performance of designated programs while providing leadership and mentorship to global clinical study managers. They act as a key point of escalation and collaborate with cross-functional teams to drive disease and asset strategy.
The GCO Program Lead is responsible for the strategic operational planning and clinical execution of designated oncology programs. This role involves leading global clinical study managers, managing program budgets, and collaborating cross-functionally to ensure high-quality delivery of clinical trials.
The Associate Director will drive cross-functional commercial and medical initiatives while serving as a strategic partner to the North America leadership team. They are responsible for structuring complex business challenges, developing actionable strategies, and implementing AI-enabled workflows to improve organizational productivity.
The Senior Director will lead the strategy, development, and adoption of digital products to optimize study budget, resource, and cost planning across global R&D. This role involves partnering with cross-functional teams to integrate AI and advanced analytics into R&D workflows while driving product lifecycle management and organizational capability.
The Senior Associate plans, tracks, and executes U.S. regulatory submissions to the FDA, serving as the primary operational liaison between strategy and publishing teams. They are responsible for ensuring all submissions are accurate, compliant, and delivered on time while maintaining version control and document integrity.
The Medical Science Liaison will serve as a scientific expert, facilitating data dissemination and building strategic relationships with healthcare providers and academic institutions. They will also support clinical pipeline development by coordinating research activities and providing internal stakeholders with critical clinical and scientific insights.
The Brand Manager is responsible for developing and implementing the local marketing strategy for onco-hematology products in France. They will lead cross-functional teams to execute tactical plans, manage budgets, and ensure alignment with global strategies to maximize brand performance.
