Manager, Medical Information and Review

Takeda Pharmaceuticals; Zürich; Hybrid; CHF 90’000 - 130’000; Vollzeit

Zusammenfassung

Takeda Pharmaceuticals is seeking a Medical Information Manager to oversee regulatory compliance for product approvals and amendments. The successful candidate will lead teams in managing medical information, ensuring adherence to policies while contributing to the mission of enhancing patient health. Join a patient-focused company that values innovation and integrity across healthcare.

Qualifikationen

• Bachelor's Degree required with a minimum of 1 year relevant experience.
• Experience in regulatory compliance and managing medical information.

Aufgaben

• Ensure compliance with regulatory policies and guidelines.
• Lead and mentor medical information teams.
• Develop comprehensive medical documents and presentations.

Kenntnisse

Medical information management

Regulatory compliance

Project management

Data analysis

Public speaking

Problem-solving

Stakeholder engagement

Ausbildung

Bachelor's Degree

Jobbeschreibung

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.

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

More about us:

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

This position is currently classified as "hybrid" in accordance with Takeda's Hybrid and Remote Work policy.

#LI-Hybrid

Locations

Zurich, Switzerland

Worker Type

Employee

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.

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

More about us:

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

This position is currently classified as "hybrid" in accordance with Takeda's Hybrid and Remote Work policy.

#LI-Hybrid

Locations

Zurich, Switzerland

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

About the company

Hope and empathy. These two words are not often associated with pharmaceutical companies. But here at Takeda, our people are motivated to serve patients with integrity, respect, and empathy. Driven by our mission, we seek to bring hope of better health and a brighter future to those we impact. To do this, we focus on our chosen core therapeutic areas:OncologyGastroenterologyNeuroscienceDevelop life-saving vaccinesNo matter the region, business unit, function, or team, everyone at Takeda matters. Every one of our employees is a vital contributor to our bold, inspiring mission.

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