Regulatory Affairs Associate - Azuqueca de Henares, Castile-La Mancha

Revisar e interpretar las normas reglamentarias relacionadas con los productos y procedimientos de la empresa. · Recopilar y revisar la documentación necesaria para la presentación de nuevos productos a los licenciatarios/afiliados locales. · ...

The Associate Director Medical Affairs Tryngolza sits within the global Tryngolza medical affairs and clinical development (MACD) team and is responsible for supporting the execution of the global medical plan for the assigned product in collaboration with the rest of the global ...

Sobi encourages you to change the statistic of applying only when meeting 100% of qualifications and apply for this Associate Director Medical Affairs position in Tryngolza medical affairs. · ...

The Associate Director Medical Affairs Tryngolza sits within the global Tryngolza medical affairs and clinical development (MACD) team and is responsible for supporting the execution of the global medical plan for the assigned product in collaboration with the rest of the global ...

The Global Associate Director Medical Affairs (GADMA) has scientific and working knowledge in their area of responsibility and responsible for supporting execution of the Global Medical and Scientific Affairs (GMSA) portion for their assigned Therapeutic Areas (TA) or across area ...

++The Regulatory Affairs Specialist is responsible for identifying and obtaining scientific, engineering, and regulatory information for review. This position works with the regulatory authorities to ensure compliant market access. · +Coordinate acceptance and management of reque ...

The Regulatory Affairs Specialist is responsible for identifying and obtaining scientific, engineering, and regulatory information for review, preparation, and maintenance of technical documentation for submission to regulatory authorities in the countries/regions where the compa ...

The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions. · Coordinates regulatory timelines an ...

Sobi offers the opportunity to work at an international pharmaceutical company focused on specialty pharmaceuticals meeting the high medical needs of rare disease patients. · Keep overview over processes and agreements involving medical information · Stay informed about Medical ...

The Medical Information Specialist will be responsible for managing medical information processes at HQ and affiliates. They will stay informed about related systems and provide high-quality responses to internal and external customers. · ...

We analyse the market to find out exactly what patients need, and then we provide pain treatments that improve their lives – while creating value for Grünenthal. · We strive to make progress towards our vision of a world free of pain – every single day, one patient at a time. · W ...

As Regulatory Affairs Trainee you will develop yourself in supporting the activities of the EMEA (Europe, Middle East and Africa) Regulatory Affairs team. · GTM activity at the level of Iberia (Spain and Portugal); product notifications, communications with National CA, support t ...

As Regulatory Affairs Trainee you will develop yourself in supporting the activities of the EMEA (Europe, Middle East and Africa) Regulatory Affairs team. · ...

The Regulatory Affairs Specialist is responsible for identifying and obtaining scientific, engineering, and regulatory information for review, preparation, and maintenance of technical documentation for submission to regulatory authorities in the countries/regions where the compa ...

This position is responsible for the full scope of public affairs responsibilities in Spain and Portugal, developing and executing a clear, compelling and high-impact government affairs, advocacy and media relations strategy, aligned with our business goals and priorities. · Deve ...

The Boeing Company is seeking a Senior or Expert Regulatory Affairs Engineer for Europe.We're committed to fostering an environment for every teammate that's welcoming, respectful and inclusive, with great opportunity for professional growth. · The successful candidate will have ...

+ Job summary: As a key leader in the Market Access and Pricing function, you will drive strategy planning and execution of market access initiatives to support successful launch of Aficamten. · + Responsibilities:Develop national market access strategies tailored to Spanish heal ...

Cytokinetics is seeking a Senior Director of Market Access for Spain to drive strategy planning and execution of market access initiatives to support the successful launch of Aficamten in 2026. · ...

The position is responsible for managing a professional Field Medical Team team to generate outstanding performance in the defined therapeutic area. · ...

Syneos Health is seeking a Principal Medical Writer to join their team. · ...