Director, Regional Regulatory Strategist- Id

**The Role**: The Director, Regional Regulatory Strategist - ID will have the opportunity to lead the regulatory strategy with the European Medicines Agency (EMA), act as the regulatory strategy partner for International countries, and provide regulatory support to the VP, Regulatory Affairs - International. This is a new role intended for a forward-looking,...

**At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our...

**The Role**: Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners...

**The Role**: The Manager of Regulatory Strategy-International based in Basel, Switzerland will have the opportunity to provide regulatory support to the Director, Regulatory Affairs-Regional Regulatory Strategist, - EU & International. This is a newly created role intended for a forward looking, creative and agile regulatory manager able to anticipate and...

**The Role**: **Here's What You’ll Do**: Develop and contribute to content, format and accountability for regulatory submissions and related supplements and amendments, including EMA regulatory documents such as meeting requests, briefing books, orphan drug designations, DSURs, MAA etc.) Work with the International local regulatory leads in Canada, Asia,...

**At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our...

**The Role**: **Here's What You’ll Do**: Develop and contribute to content, format and accountability for regulatory submissions and related supplements and amendments, including EMA regulatory documents such as meeting requests, briefing books, orphan drug designations, DSURs, MAA etc.) Work with the International local regulatory leads in Canada, Asia,...

Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine?Join us as an **Associate Director, GRA Regional Compliance - EU/Extended EU**, based in Zurich. **Here, you will be a vital contributor to our inspiring, bold mission.** **OBJECTIVES**: - Provide direction and leadership in the identification,...

General Description: The Director Regulatory Affairs will be responsible for developing and implementing regulatory strategies for the designated program to secure and maintain marketing authorization in line with business objectives, and in coordination with key internal stakeholders. Essential Functions of the job: - Act as the representative of European...

**THE POSITION**: This role of is the senior most regulatory role within EPD in the Emerging Market business unit_. _As a leader, the role of the Director, Regulatory Affairs is to combine knowledge of scientific, regulatory and business issues to support and partner the business by ensuring the successful development, manufacture and distribution of...

**The Role**: Leads and continues to build the Clinical Trial Application (CTA) regulatory group, responsible for providing effective operational and regulatory support for assigned regulatory clinical trial submissions and maintenance activities, including preparation and submission of regulatory dossiers, and maintenance of regulatory databases and...

**The Role**: The Manager of Regulatory Strategy-International based in Basel, Switzerland will have the opportunity to provide regulatory support to the Senior Director, Regulatory Affairs Strategy, Infectious Disease. This is a newly created role intended for a forward looking, creative and agile regulatory manager able to anticipate and address the...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 113,000 colleagues serve people in more than 160 countries.Abbott...

Job SummaryWe are seeking an experienced Safety Director to join our team. The successful candidate will be responsible for delivering knowledge on the safety profiles of our medicines, defining how to manage risks to patients and coordinating pharmacovigilance system activities.Key ResponsibilitiesDeveloping Safety Strategies: You will develop and implement...

REGULATORY AFFAIRS Associate Director, Europe (with focus on Switzerland) Regulatory Affairs, Basel, Switzerland Reports To: Director, Team Lead of EU Regulatory Affairs **Job Description**: The (Swiss) Regulatory Affairs lead will report to the team lead of Regulatory Affairs Europe and will have dotted line reporting to the Swiss General Manager. The...

**At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our...

Contract Type: Permanent Closing date: Reference: VN1863 About Us Vectura Fertin Pharma’s ambition is to become a market-leading wellness and healthcare business. Formed in March 2022, the business brings together two unique organizations: Vectura, experts in inhalation technology and Fertin Pharma, experts in oral and intra-oral delivery systems. We...

About the role: As the Director Regulatory Toxicology, you and your team will work closely with the Scientific Innovation leadership and play a pivotal role in the development and success of our Innovation Centre in this dynamic and quickly evolving market. - This is a real opportunity to play a central role in ensuring the continuation and ongoing...

Company Overview: BeiGene, Ltd. (NASDAQ: BGNE; HKEX: 06160) is a global, commercial-stage, research-based biotechnology company focused on molecularly targeted and immuno-oncology cancer therapeutics. With a global team of over 9,000 employees located in China, the United States, the EU, the UK, Switzerland and Australia, BeiGene is advancing a pipeline...

**The Role**: Reporting to the Director Quality Systems & Compliance the AD Regulatory Compliance will be responsible to be the liaison function between Quality and the Regulatory CMC functions of Moderna. The role will implement and continuously improve required processes to ensure the compliance of Moderna’s product with the registered...