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The Associate Director oversees R&D HCP engagement, ensuring compliance, process implementation, and operational excellence while leading a team and engaging with stakeholders.

The Senior Manager, Quality Centers of Excellence leads the development and execution of prioritized CoEs, drives initiatives, establishes governance structures, tracks performance metrics, and collaborates with global teams for operational excellence.

Manage the day-to-day operations of HCP engagement, contracting processes, and maintain compliance and documentation standards while supporting internal stakeholders.

Manage end-to-end contracts for Global Medical Affairs, including drafting, negotiating, and ensuring compliance. Liaise with vendors and stakeholders, oversee vendor performance, and implement process improvements.

Manage the Learning Management System (LMS) operations, oversee training initiatives, analyze platform usage, and collaborate with management to enhance learning solutions.

The Associate Director will develop and implement strategic plans, oversee operations, improve processes, manage budgets, and collaborate across functions in Global Medical Affairs.

The Associate Director will optimize GMP processes, lead cross-functional quality initiatives, ensure compliance, and enhance quality system performance globally.

The Director leads market access strategies, developing value propositions, managing payer marketing, and collaborating with brand teams to drive initiatives while managing resources and engaging stakeholders.

The Senior Manager will oversee strategic initiatives for Medical Affairs, focusing on external stakeholder engagement and cross-functional collaboration. Responsibilities include strategic planning, developing engagement models, and ensuring compliance with regulations.

The Senior Manager oversees quality assurance for biologics manufacturing, ensuring compliance with GMP standards, managing contract manufacturers, and leading quality system records for clinical and commercial products.