Empleos de maa en Barcelona

CTC Resourcing Solutions seeks an experienced EU Regulatory Lead to support planning, preparation and submission of a Marketing Authorization Application (MAA) to the EMA. This is a 6–12 month contract with 100% remote work across Europe and 50%–70% FTE. You will provide strategic EU regulatory leadership, interact with EMA and other European...

Director, Principal Patient Safety Scientist Oncology Location: Barcelona, Spain (on-site) 3 days working from the office and 2 days working from home. AstraZeneca is a global, science‑led, patient‑focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most...

Director, Principal Patient Safety Scientist Oncology Location: Barcelona, Spain (on-site) 3 days working from the office and 2 days working from home. AstraZeneca is a global, science‑led, patient‑focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s...

Oxford Global Resources is seeking a Global CMC Regulatory Affairs Manager Consultant to support as external contractor on behalf of Oxford a top leading pharma company to support headquarters in Barcelona through our consulting services division. Key Responsibilities Provide CMC regulatory insight and advice to multidisciplinary teams, as well as CMC...

## ASSOCIATE DIRECTOR, REGULATORY AFFAIRSSolicitarremote type: R&D & Medical Affairslocations: SANT FELIU DE LLOBREGATtime type: Full timeposted on: Publicado hace 4 díasjob requisition id: Estamos construyendo el futuro de la dermatología médica centrándonos en las necesidades no cubiertas de los pacientes y dando a las personas el espacio para pensar...

## ASSOCIATE DIRECTOR, REGULATORY AFFAIRSBewerbenremote type: R&D & Medical Affairslocations: SANT FELIU DE LLOBREGATtime type: Full timeposted on: Vor 4 Tagen ausgeschriebenjob requisition id: Si desea saber un poco más sobre esta oportunidad, o está considerando presentar su candidatura, por favor, lea la siguiente información del puesto.**Warum...

Location: Barcelona - Spain (3 days working from the office and 2 days working from home) Introduction to the role Turn groundbreaking science into clear, compelling regulatory narratives that accelerate patient impact. We’re hiring a Associate Director/Director, Clinical Regulatory Writing, to lead communications strategy and delivery for our...

Location: Barcelona - Spain (3 days working from the office and 2 days working from home) Introduction to the role Turn groundbreaking science into clear, compelling regulatory narratives that accelerate patient impact. We’re hiring a Associate Director/Director, Clinical Regulatory Writing, to lead communications strategy and delivery for our...

We’re building the future of medical dermatology by focusing on unmet patient needs and giving people the space to think independently, take ownership and make an impact that matters.Our purpose is simple: to transform patients’ lives by addressing real needs. We work with care, act with courage, keep things simple and focus our innovation where it...

Director, Principal Patient Safety Scientist Oncology Location: Barcelona, Spain (on-site) 3 days working from the office and 2 days working from home. AstraZeneca is a global, science‑led, patient‑focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most...

We're building the future of medical dermatology by focusing on unmet patient needs and giving people the space to think independently, take ownership and make an impact that matters. Our purpose is simple: to transform patients' lives by addressing real needs. We work with care, act with courage, keep things simple and focus our innovation where it makes...

Our client provides cross-functional consulting services, to support pharma, biotech and medtech organizations to achieve sustainable success and continuously uphold industry standards while navigating dynamic and international regulatory landscapes across the lifecycle of medicinal products, devices, IVDs and combination products. They also provide...

We’re building the future of medical dermatology by focusing on unmet patient needs and giving people the space to think independently, take ownership and make an impact that matters.Our purpose is simple: to transform patients’ lives by addressing real needs. We work with care, act with courage, keep things simple and focus our innovation where it...

   CONVOCATÒRIA INTERNA/EXTERNA nº 2023-24La Fundació de Gestió Sanitària de l’Hospital de la Santa Creu i Sant Pau precisa incorporar UN/UNA:   2023-24 FACULTATIU/VA ESPECIALISTA EN MEDICINA NUCLEAR Requisits: Títol de Llicenciat/da en Medicina i CirurgiaTítol d’especialista en Medicina NuclearExperiència en valoració de la...

Location: Barcelona - Spain (3 days working from the office and 2 days working from home)Introduction to the roleTurn groundbreaking science into clear, compelling regulatory narratives that accelerate patient impact. We’re hiring a Associate Director/Director, Clinical Regulatory Writing, to lead communications strategy and delivery for our...

Location: Barcelona - Spain (3 days working from the office and 2 days working from home)Introduction:  The Associate Director, Patient Safety Scientist role works collaboratively with the Global Safety Physician (GSP) and (Senior/Principal) PV Scientist with the review of safety data and related documents for potential safety issues.  He/she has the...

Location: Barcelona - Spain (3 days working from the office and 2 days working from home)Introduction to the roleThe Director, International CMC Regulatory Affairs – Cell and Gene Therapy provides strategic, operational and tactical CMC regulatory leadership for a portfolio of cell and gene therapies and biologics across clinical development, registration,...

Discover International in Spain seeks a Senior Director, Regulatory Affairs to lead global regulatory strategy for oncology programs and oversee end-to-end submissions from development through lifecycle management. You will drive Health Authority engagements, coordinate cross-functional teams across Clinical, CMC, Safety and Commercial, and ensure timely...

Location: Barcelona - Spain (3 days working from the office and 2 days working from home) Inscríbase (haciendo clic en el botón correspondiente) después de revisar toda la información relacionada con el trabajo a continuación. Introduction to the role Turn groundbreaking science into clear, compelling regulatory narratives that accelerate patient...

The Senior Director, Regulatory Affairs is responsible for leading regulatory strategy and execution for assigned development programs, with a primary focus on oncology and broader disease areas as needed. This role will serve as the Global Regulatory Lead for designated assets and will be accountable for end-to-end regulatory leadership from early...