Manager, Medical Information and Review(m/w/x)

# Manager, Medical Information and Review **Zurich, Switzerland** | **Full time** ## Job Description **About the role:** The Medical Information, Manager is responsible for ensuring that Takeda gains regulatory approval for new products and product amendments, and maintains the currency of product licenses and permits. By monitoring regulatory developments and ensuring compliance, this role supports the organization's mission to bring better health to people and a brighter future to the world. As an experienced professional, you specialize in solving various complex problems, sometimes referring to established precedents and policies. Your work involves analyzing diverse data and selecting appropriate methods for solutions, while networking with senior professionals in your field. You possess a complete understanding of principles, concepts, and industry practices, exerting some influence on organizational objectives. You often work independently under general direction, occasionally leading small project teams, and may represent the organization in contractual or project matters, interacting with senior internal and external personnel. You might also participate in training junior staff. **How you will contribute:** \* Develop and manage comprehensive medical information with minimal guidance \* Design and review clinical protocols, ensuring alignment with strategic and regulatory requirements \* Ensure medical activities comply with all regulatory policies and guidelines \* Lead and mentor teams, providing direction and support in Medical Information tasks \* Represent the organization in negotiations and communications with external stakeholders \* Manage projects within the Medical Information scope, ensuring timely and effective completion **Skills and qualifications**: \* Develops and manages comprehensive medical information with minimal guidance \* Designs and reviews clinical protocols, ensuring alignment with strategic and regulatory requirements \* Ensures medical activities comply with all regulatory policies and guidelines, enhancing product strategy implementation \* Leads and mentors teams, providing direction and support in Medical Information tasks \* Represents the organization effectively in negotiations and communications with external stakeholders \* Manages projects within the Medical Information scope, ensuring timely and effective completion \* Produces detailed medical documents and communications materials independently \* Communicates complex medical information clearly and effectively \* Maintains high attention to detail in all tasks, ensuring accuracy and compliance \* Develops and delivers impactful presentations, engaging a variety of stakeholders \* Applies pharmacovigilance principles to monitor drug safety effectively \* Utilizes knowledge of biotechnology and health economics to support product information and outcomes research **Minimum Requirements/Qualifications:** * Bachelor's Degree and a minimum of 1 year relevant experience ## Locations Zurich, Switzerland ## Worker Type Employee ## Worker Sub-Type Regular ## Time Type Full time