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The Associate Director of Site Management leads site management activities, ensuring effective clinical trial execution and compliance, while managing and developing a team of site managers.

The National Account Director, GPO will expand relationships with McKesson's GPO, develop access strategies for oncology practices, and coordinate internal stakeholders to ensure product access and patient care improvements.

The Programming Manager leads programming activities for clinical studies, ensuring data quality and adherence to standards. Responsibilities include developing programs, supporting data management, and reviewing submissions, while fostering collaboration and maintaining regulatory knowledge.

Lead the development and maintenance of global labeling documents, advise on global labeling strategies, and monitor regulatory environment. Manage projects and support regulatory policy deliverables.

Lead programming for clinical trials, ensuring programming specifications and consistency across trials, mentoring employees, and overseeing vendor programming activities.

The Associate Director provides statistical expertise for clinical drug development, engages with regulators, leads strategies, collaborates on trial designs, and ensures proper analyses and data handling.

The Associate Director of Biostatistics leads statistical strategies in drug development, collaborates with stakeholders, and oversees trial-level analyses, ensuring compliance with regulatory standards.