The Central Monitor oversees clinical trials via data surveillance and centralized monitoring, ensuring data quality and regulatory compliance.

The Lead Central Monitor oversees clinical trial monitoring by managing a team, developing strategies, ensuring data integrity, and fostering collaboration. They drive risk management and process improvements while supporting clinical trial teams in their execution.

Provide strategic legal counsel in the pharmaceutical sector, manage legal risks, negotiate agreements, lead litigation, and develop team policies.

The ESG FRA Process & Project Expert coordinates ESG reporting projects, supports governance, ensures compliance with regulations, and enhances non-financial reporting processes.

The Global Program Clinical Head leads clinical programs in neuroscience, overseeing strategies and execution for regulatory approvals and market access, interacts with stakeholders, and ensures team development.

The Associate Director leads statistical programming for clinical trials, ensuring collaboration, resource allocation, and compliance while mentoring team members and developing documentation.

The Head of Scientific Learning & Capability leads the design and implementation of capabilities across International Medical Affairs, enhancing performance through learning strategies and programs while collaborating with cross-functional teams and managing external partnerships.

The Global Program Associate Director will manage global drug development projects, facilitating strategies, communication, and issue resolution while ensuring effective operation of the Global Program Teams.

The Senior Principal Statistical Programmer leads statistical programming for clinical studies, ensures compliance with standards, supervises programmers, and delivers high-quality datasets and outputs.

Provide strategic legal counsel and risk management for CLS Operations, support compliance, manage BD/M&A activities, oversee regulatory materials, drive innovation, and engage with various stakeholders.

The role involves developing and implementing HEOR strategies, ensuring access evidence needs, delivering impactful HEOR evidence, and collaborating with interdisciplinary teams to maximize product value for patient access.

Lead Clinical Development operational strategy, oversee processes, systems and quality frameworks, drive process improvements, enable inspection readiness, manage cross-functional initiatives, and develop the Business Solutions team to support Phase 2/3 trials and regulatory compliance.

Lead statistical work and innovative trial designs in collaboration with clinical teams to enable quantitative decision making across projects.

The Functional Excellence Lead drives operational advancement in monitoring practices, ensuring alignment with RBQM principles, and optimizing trial efficiency through innovative techniques and stakeholder collaboration.

The Senior Global Process Owner leads the design and management of risk-based quality management processes in clinical trials, ensuring compliance and continuous improvement.

The Senior Global Process Owner leads the end-to-end clinical trial process, ensuring compliance, governance, and continuous improvement through collaboration and process optimization.

The Clinical Development Director leads clinical programs, ensuring delivery of clinical goals, collaborating across teams, managing trial data, and contributing to regulatory documents amidst a focus on patient safety.

Lead statistical programming activities for clinical studies, ensuring compliance with standards and providing high-quality deliverables. Collaborate with teams and mentor programmers.

The Study Start-Up Senior Lead is responsible for leading global SSU activities, managing teams, and ensuring timely trial document preparation for submissions and site activations.