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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.

The Manager/Sr. Manager will enhance site relationships and drive clinical trial efficiency, while ensuring compliance, communication, and quality in trial conduct.

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.