The Clinical Study Manager is responsible for planning, executing, and managing clinical studies while providing leadership to multidisciplinary program teams. They oversee vendor performance, manage trial budgets, and ensure compliance with regulatory standards and study protocols.
The Associate Director will develop and execute global clinical supply chain strategies, including forecasting, demand planning, and inventory management. They will also oversee external vendors, ensure regulatory compliance, and lead cross-functional collaboration to support clinical trial timelines.
The Sales Area Director will lead and manage four Regional Business Directors and their teams to accelerate the growth of Yutrepia and Treprostinil Injection in the PAH marketplace. This role involves extensive field-based coaching, strategic business planning, and building high-level relationships with Key Opinion Leaders.
The Sales Area Director will lead and manage four Regional Business Directors and their teams to accelerate the growth of Yutrepia and Treprostinil Injection. The role involves extensive field-based work, KOL development, and strategic alignment with senior leadership to drive national sales performance.
The Medical Information Manager is responsible for authoring and maintaining standard medical response documents and managing the company's medical information repository. They also provide medical expertise during the review of promotional and scientific materials to ensure regulatory compliance and accuracy.
The Medical Science Liaison serves as a scientific expert to facilitate clinical exchange and build relationships with key opinion leaders in the PAH and PH-ILD communities. They are responsible for executing strategic engagement plans, gathering medical insights, and supporting clinical trial recruitment efforts.
The Executive Director will provide strategic and scientific leadership for pharmacokinetic and pharmacometrics activities across the drug development portfolio. They will translate clinical pharmacology principles into actionable development strategies while collaborating with cross-functional teams to support evidence-based decision making.
The Senior Manager, Regulatory Affairs supports the development and execution of regulatory strategy for rare disease and cardio-pulmonary drug-device combination products. They coordinate global regulatory submissions, manage health authority interactions, and collaborate with cross-functional teams to ensure compliance throughout the product lifecycle.
The Manager, Legal Operations is responsible for driving process optimization, legal technology implementation, and contract administration to enhance the efficiency of the Legal and Compliance department. This role also manages departmental budgets, outside counsel relationships, and cross-functional initiatives to ensure alignment with corporate strategy.
The role is responsible for growing sales and managing commercialization within a specific geographic territory. This includes serving as a resource for healthcare professionals and ensuring adherence to compliance laws and policies.
