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Manage resource allocation and ensure compliance in clinical trials. Oversee project management, documentation, and maintain adherence to quality standards.

The Clinical Development Director leads clinical activities, ensuring successful trial execution, and collaborates with stakeholders while mentoring team members.

The Vendor Program Strategy Director oversees vendor activities for clinical studies, ensuring compliance with regulations, managing supplier performance, and defining program strategies in collaboration with various stakeholders.

As Director, you'll lead strategic planning and execution of clinical programs, manage resources, ensure compliance, and drive team performance across global trials.

Leads development of scientific communication platforms aligned with therapeutic areas, manages publication teams, and develops medical education plans. Oversees scientific communications for congress events and ensures regulatory compliance.

The Risk Surveillance Lead ensures RBQM practices, oversees quality risk governance in clinical trials, and collaborates cross-functionally to enhance trial quality.

The Associate Director, Statistical Programming leads statistical programming for clinical trials, ensuring collaboration, quality, and compliance while mentoring teams and overseeing resource allocation.

Manage TMF documentation for M&A projects, oversee transitions, develop processes, and ensure compliance in clinical document management.

The Global Program Clinical Head oversees clinical programs, leading teams in strategy, execution, and regulatory compliance for drug development. Responsibilities include designing clinical studies, ensuring drug safety, and collaborating with stakeholders for successful market access.

The Solution Design Associate Director will translate business challenges into innovative solutions, lead technical teams, and enhance business operations through strategic design and project management.