Provide comprehensive executive administrative support, manage calendars, arrange travel, coordinate meetings, and improve team efficiency in a complex global organization.

The Director, CX, Campaign Touchpoints will lead creative campaign production, manage agency partnerships, and drive customer engagement through storytelling across marketing materials.

The Head of Study Grants leads the Grant Plan strategy and ensures accurate FMV assessments for clinical trials and studies. This role involves budget forecasting, site contracting, and collaboration with various teams to enhance operational efficiencies. The position also entails managing and developing teams, driving innovative processes, and ensuring compliance with regulations.

Lead PK strategy for biologics projects, analyze and interpret PK/PD data, author clinical documents, and enhance visibility through publications.

The Principal Scientist II/Senior Principal Scientist will lead and implement PK strategies for drug candidate progression, analyze PK/PD data, and contribute to project planning and approval processes.

The Global Program Associate Director leads project management for drug development, coordinating teams and strategies to ensure effective program execution and communication.

Oversee global feasibility assessments, analyze clinical trial data, provide modeling for recruitment projections, and collaborate with clinical teams.

The Senior Principal Biostatistician will provide statistical solutions in HTA, lead collaborations, ensure timely deliverables, and communicate findings clearly.

The Associate Director Biostatistics leads statistical solutions for HTA and reimbursement activities, managing projects and collaborating with various teams to drive decision-making.

The Global FCC Process Expert is responsible for overseeing financial E2E process risks, collaborating with GPOs, and ensuring compliance accountability in S2P, T&E, and PRO processes.

The Associate Director of Biostatistics provides leadership in statistical strategy for clinical trials, ensures data integrity, and collaborates across teams for effective clinical development and regulatory submissions.

The Associate Director Pharmacometrics will drive pharmacometrics strategy for clinical programs, develop plans for regulatory submissions, provide strategic leadership, and integrate pharmacometrics information for drug development milestones.

The Senior Principal Statistical Programmer leads statistical programming for clinical studies, ensuring quality deliverables and compliance with industry standards, while supervising programming teams.

Lead pharmacometrics efforts for clinical development, providing strategic expertise and technical support for regulatory submissions and evidence generation.

As an Associate Director of Biostatistics, you will drive statistical strategies for early clinical trials, mentor quantitative scientists, and represent the department in decision-making processes.

The Senior Principal Biostatistician oversees statistical work for clinical trials, collaborates on trial designs, and provides statistical expertise. Requires extensive experience in statistics and clinical trials.

Lead statistical programming for clinical studies, overseeing programming standards, coordinating teams, ensuring quality deliverables, and complying with industry standards.

The role includes providing statistical support for real-world evidence studies, developing protocols and analysis plans, managing studies, and training others on relevant methods.

The role involves statistical support for real-world evidence studies, designing and analyzing studies, and contributing to regulatory documents while managing projects and stakeholders.

The Marketing Director for Solid Tumours will oversee brand strategy, P&L management, product launch, team leadership, and operational direction in a hybrid environment.