Ofertas de trabajo para: - REGULATORY AFFAIRS MANAGER

A challenging opportunity to join the team based in Madrid Affiliate Office, as a Clinical Trial Manager Associate (CTMA), to be responsible for the management of post-authorization studies across different therapeutic areas.Plays a vital role in successful implementation and support of Company s Sponsored, Collaborative (CO) and Investigator-Sponsored Research (ISR) projects.Client Details A research-based bio pharmaceutical company dedicated to deliver life-saving therapies to patients in need...

Buscamos un/a Regulatory Affairs para importante empresa farmacéutica situada en Barcelona. Empresa de producción y comercialización de productos sanitarios, especializados en la terapia de infusión y nutrición clínica.Las funciones a realizar serán:- Preparación de paquetes de variación para la posterior aprobación de los cambios de CMC para productos de Pharma bajo la supervisión RA Manager. - Determinación de la estrategia para el despliegue óptimo de los cambios de CMC bajo la supervisión de...

Homeworking Flexibility : Spain Im currently working with a leading consultancy that is going through significant changes as they implement a new strategy to become the go to consultancy within Regulatory and Development. As a part of this strategy, they are now recruiting for a Senior Regulatory Affairs Manager to focus on Active Substance Registrations. This is an exciting opportunity to be a key player in the growth of a high potential business. You will be coordinating a variety of regulator...

The Functional Manager (FM) position is accountable for the successful regional or country execution of all phases of clinical trials for an assigned Therapeutic Area(s) or specific role(s), including resource allocation, adherence to timelines and budget, compliance with all GCO SOPs, policies and regulatory requirements. This position is responsible for the direct functional management of Local Trial Managers, Site Managers and Investigator Document Associates/Clinical Trial Assistants and oth...

Acerca de esta páginaMedical Affairs Manager/Madrid/MAF Nuestro Cliente, empresa farmacéutica multinacional, busca un MEDICAL AFFAIRS MANAGER.Es imprescindible que el/la candidata/a sea Licenciado/a en Medicina y tenga un alto nivel de inglés. Functions/Responsibilities Providing accurate clinical and technical information for the Company s products. Contributing to new product development and product launches Revision and approval of promotional activities in accordance with Industry Code of Pr...

Acerca de esta páginaDesde ADEAS HR, selecciona a un/a IT SUPPORT SPECIALIST a nivel global de grupo para una importante multinacional farmacéutica ubicada en Sant Cugat, Barcelona. Como miembro del Dpto. Regulatory Affairs Service Center serás responsable de garantizar el soporte a los usuarios a nivel internacional, implementaciones y resolución de incidencias para las aplicaciones del área. Funciones Responsabilidades; Serás responsable de dar soporte al grupo a nivel global en relación a los...

Oferta de trabajo: Apply for job Save job » Company: Alexion Pharmaceuticals » Location: Ireland » Salary: negotiable / month » Job type: Full-Time » Posted: 4 mins ago » Category: General The Senior Specialist for External Quality will be responsible, with management support, for providing oversight of quality activities associated with drug substance, drug product and finished product manufacturing processes to contract manufacturing organizations. The Senior Specialist contributes and support...

Empleo: Apply for job Save job » Company: Salessense » Location: Ireland, Glasnevin » Salary: negotiable / month » Job type: Full-Time » Posted: 3 mins ago » Category: General The QCRA Co-Ordinator reporting to the QCRA Manager will work across the Sisk Healthcare Group to support our Quality, Compliance and Regulatory Affairs requirements. This role will require occasional travel between our offices in Dublin and Belfast. The primary purpose of the role is to manage the ongoing maintenance of o...

Regulatory/Quality Affairs Specialist, EMEA (Madrid New Madrid, Spain Regulatory Quality Assurance 9 hours ago Post Date 38 Total Views Apply for Job Recommend to a Friend Sign Up for Job Alerts ROLE ESSENTIAL DUTIES AND RESPONSIBILITIES Regulatory : * Apply regulations by supporting regulatory strategies for EMEA markets * Define, monitor, collate, and publish deliverables for submissions in coordination with divisional RA teams * Participate in regulatory submission teams * Write and/or edit s...

Company Info We are a consulting firm based in Madrid specialized in healthcare and related industries such as cosmetics, nutrition amp; food, chemicals, among others. We provide solutions covering a wide spectrum that includes marketing strategy, branding, communication and regulatory affairs to companies in the sector. We are present in Europe, America and Asia with over 500 consultants in our 19 offices, serving more than 450 clients worldwide, 60 of them in Spain. Our clients include renowne...

Who we are:Johnson Johnson Vision, through its operating companies, is committed to improving and restoring sight for patients worldwide. Since debuting the world s first disposable soft contact lens in 1987, Johnson Johnson Vision Care, Inc. has been helping patients see better through their world-leading ACUVUE®? Brand Contact Lenses portfolio. In 2017, with the addition of Abbott Medical Optics Inc., the Johnson Johnson Surgical Vision business, Johnson Johnson invested further in eye health ...

At Uber, we ignite opportunity by setting the world in motion. We take on big problems to help drivers, riders, delivery partners, and eaters get moving in more than 600 cities around the world. We welcome people from all backgrounds who seek the opportunity to help build a future where everyone and everything can move independently. If you have the curiosity, passion, and collaborative spirit, work with us, and let s move the world forward, together. About the Role As a Senior General Manager, ...

The key responsibilities of the vacancy will be:Develop the business in the aforementioned geographic areas (North of Africa and Middle East).Maintain the already existing clients.Negotiate the contract economic terms.Participate to international summits and fairs.Manage the regulatory affairs of the products in Middle East and North of Africa. The ideal candidate will:Have a technical degree.Have at least 2 years of experience with the agrochemical sector.Speak English fluently (negotiation wit...

At AstraZeneca we believe in the potential of our people and you ll develop beyond what you thought possible. We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us.To lead Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with AZ Procedural Documents, international guidelines such as ICH-GCP as well as relevant ...

Job SummaryJob Location: Canton de Vaud in Switzerland, Spain, Italy, Netherlands or BelgiumOverviewBD carries a wide range of infusion pumps, both syringe and large volume pumps, covering a range of applications from fluid administration, IV pain management, hospital and home parenteral nutrition, blood transfusion to chemotherapy. Pump sets are the crucial component in ensuring safe delivery of these fluids and medication to the patient, but are ultimately part of a system, which needs to work...

Company Info This opportunity is part of the Planet Expat Work Abroad Program, which aims to maximize your chances of joining one of the most innovative companies in Europe and Latin America. Here is more information about the hiring company: We are a consulting firm based in Madrid specialized in healthcare and related industries such as cosmetics, nutrition food, chemicals, among others. We provide solutions covering a wide spectrum that includes marketing strategy, branding, communication and...

A challenging opportunity to join the team based in Madrid Affiliate Office, as a Clinical Trial Manager Associate (CTMA), to be responsible for the management of post-authorization studies across different therapeutic areas. Plays a vital role in successful implementation and support of Company s Sponsored, Collaborative (CO) and Investigator-Sponsored Research (ISR) projects. Client Details A research-based bio pharmaceutical company dedicated to deliver life-saving therapies to patients in ne...

Sr Manager Market Access For Current Gilead Employees and Contractors: Please log onto your Internal Career Site to apply for this job. Job Description Specific Responsibilities and skills The Senior Market Access HEOR Managerwill be responsible for the development and communication of the value proposition (including pricing and reimbursement) for the Gilead product. * Work with HQ to adapt core models commissioned by them * Commission or create core models on the initiative of International, w...

The key responsibilities of the vacancy will be:Develop the business in the aforementioned geographic areas (North of Africa and Middle East).Maintain the already existing clients.Negotiate the contract economic terms.Participate to international summits and fairs.Manage the regulatory affairs of the products in Middle East and North of Africa. The ideal candidate will:Have a technical degree.Have at least 2 years of experience with the agrochemical sector.Speak English fluently (negotiation wit...

The key responsibilities of the vacancy will be: -Develop the business in the aforementioned geographic areas (North of Africa and Middle East). -Maintain the already existing clients. -Negotiate the contract economic terms. -Participate to international summits and fairs. -Manage the regulatory affairs of the products in Middle East and North of Africa. -Growing and top agrochemical company - Growing and top agrochemical company The ideal candidate will: -Have a technical degree. -Have at least...