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Manage regional study delivery, oversee clinical operations, ensure compliance and inspection readiness, and collaborate with stakeholders to meet study goals.

The Associate Director will lead the development of regulatory strategies, manage CMC submissions, and ensure compliance with health authority requirements for small molecules.

The Associate Director leads and mentors clinical study managers, ensuring alignment with organizational goals and quality standards while managing study performance and resources.

The Manager of Clinical Supply Chain oversees drug supply activities for clinical programs, develops supply plans, manages inventory, and ensures compliance with regulations.

The Head of Americas for Global Clinical Operations leads strategic management of clinical trials, oversees project delivery, and ensures compliance across regions. The role involves mentoring teams, enhancing operational efficiency, and establishing organizational standards in clinical development to drive successful trial execution.

The Clinical Research Manager oversees clinical monitoring, manages the CRA team, ensures compliance with regulations, and supports site relationships and performance.

The role involves managing regional clinical operations, ensuring study delivery and compliance, and collaborating with internal and external stakeholders. It includes planning timelines, managing budgets, leading teams, and handling quality assurance audits for clinical studies.

The internship involves supporting talent development initiatives including organizing training sessions, managing LMS, data analysis, and general HR support.

The intern will collaborate with statisticians to conduct analysis using AI and machine learning techniques, implementing models and analyzing clinical data.

Lead statistical programming for multiple clinical development projects, ensuring quality and compliance while collaborating with cross-functional teams and overseeing data analysis.