The Senior Clinical Study Lead is responsible for the global execution of complex clinical trials, ensuring compliance, managing study timelines and budgets, overseeing vendor engagements, and leading the clinical study teams.

Lead global execution of large/complex hematology clinical trials from design through close-out. Accountable for timelines, budget, regulatory compliance, CRO/vendor management, site selection and monitoring, data quality, supplies forecasting, audit/inspection readiness, team and line management, and process improvements.

Lead planning, coordination, and delivery of commercial meetings, congresses, and trainings across multiple geographies. Manage vendors, budgets, contracts, compliance, attendee operations, SOPs, KPIs, and event platforms while partnering with cross-functional and alliance teams to ensure measurable impact and field readiness.

This role involves driving market access strategies for rare disease treatments in the EU, engaging with healthcare policymakers, and collaborating with cross-functional teams to ensure access.

The Senior Manager leads regulatory submission compliance, ensuring documentation aligns with global requirements, managing CMC processes, and coordinating cross-functional activities to support clinical trial releases.

The Director Program Operations Leader manages clinical operations, overseeing quality, budgets, and timelines for oncology clinical trials, while ensuring compliance with regulations and SOPs.

Coordinate and support CMC regulatory submissions for CTAs, ensuring compliance with global health authority requirements and facilitating communication among stakeholders.

The Associate Director in CMC Regulatory Affairs leads global regulatory strategies for combination products and medical devices, mentors staff, and interacts with global regulatory authorities.

Responsible for managing and executing procurement activities in global clinical CRO category, negotiating supplier contracts, and ensuring compliance with regulations.

The Program Operations Leader oversees complex clinical programs, ensuring quality, timelines, and budgets are met. They manage clinical operations, staff development, and vendor relationships, providing operational insights and driving strategic planning within clinical trial management.

The Director POL leads operational strategy and execution for complex clinical programs, ensuring quality, timelines, and budgets for clinical studies. They manage clinical operations staff, interact with stakeholders, and drive decision making for successful study outcomes.

Lead quality management in clinical trials, ensuring compliance, advising stakeholders, and driving quality initiatives within Global Development Quality systems.

As a Manager Global Procurement, oversee procurement strategies, manage supplier relationships, negotiate contracts, ensure compliance, and drive cost-saving initiatives in the biopharmaceutical sector.

The Senior Director Regional Marketing leads the regional marketing strategy for Oncology, ensuring alignment between country teams and global leadership, while driving portfolio performance and supporting launches.

The Associate Director will lead insights and analytics for Rare Diseases, overseeing market research, data management, and collaboration across teams to drive business decisions.

The Director, Program Operations Leader oversees clinical operations for trials, ensuring quality, timelines, and budgets are met. Responsibilities include management of staff, budget oversight, stakeholder communication, and operational insights on clinical program development.

The Senior Manager RBQM Data Analyst oversees centralized monitoring activities for clinical trials, utilizing data analysis tools to assess risks and operational performance, while leading process improvements and training junior staff.

The Associate Director will oversee global drug safety risk management activities, ensure compliance with regulations, manage cross-functional teams, and communicate effectively with stakeholders.