Lead global regulatory strategy for development teams, ensuring compliance with regulatory requirements and preparing key regulatory documentation while coordinating across functions and engaging with health authorities.

The Executive Director of Corporate Strategy leads strategic initiatives, collaborates across functions, informs decisions with market research, and oversees strategy implementation while managing risks associated with business operations.

This role leads digital transformation in Global Supply Chain, driving technology adoption and process automation while ensuring data governance and user-focused deployment of solutions.

The Associate Manager, Clinical Data Management oversees data management tasks in clinical studies, ensuring compliance and quality throughout study phases.

The Senior Director oversees the oncology small molecule portfolio, guiding the design and optimization of assays and leading a multidisciplinary team in drug discovery efforts.

Manage AWS infrastructure, optimize resources, automate processes, ensure security compliance, and collaborate with teams for application deployment.

The Senior Manager oversees CSC Quality activities within the Global Product Supply team, ensuring compliance with GMP standards and leading quality assurance initiatives. Responsibilities include quality oversight, regulatory inspections support, and supervising quality operations personnel.

Lead Global Development Operations, overseeing clinical trials, strategic direction, compliance, and team growth. Manage a large-scale global organization and optimize costs.

The intern will develop ELISA protocols to examine proteins in patient plasma and CSF, documenting results and generating standard operating procedures.

The Sr. Manager will oversee Clinical Data Management including line management responsibilities, resource allocation, and team development, while ensuring data quality for clinical trials.

The Associate Manager, Clinical Data Management oversees end-to-end data management tasks, supports project management, and trains junior staff across clinical studies.

The Executive Assistant to SVP coordinates administrative tasks, manages schedules, organizes events, and supports internal processes for the U.S. Policy and Government Affairs office.

Develop and document risk-based quality management strategies for clinical trials, ensuring compliance and effective risk mitigation throughout the trial lifecycle.

Responsible for laboratory operations, performing sample testing, data analysis, documentation, and assisting with equipment qualification in compliance with cGMP regulations.

The Associate Manager will oversee end-to-end Clinical Data Management tasks, ensuring data quality and compliance while collaborating with teams and coordinating project activities.

The Director, Global Trial Lead oversees global clinical trials, ensuring high-quality data and compliance while leading cross-functional teams and driving strategic initiatives.

The role involves leading strategic programs, managing projects, driving operational excellence, and ensuring compliance in cell therapy operations.

The Director, Global Trial Lead oversees global clinical trials, ensuring operational excellence and regulatory compliance while mentoring teams and fostering collaboration.

Lead global clinical trials, manage project plans and budgets, optimize operations, foster collaboration, and mitigate risks throughout the trial process.

Lead global clinical trials, collaborating with teams, managing budgets, ensuring quality and compliance, and mentoring team members.