Ofertes d'ocupació de Metge/essa a Madrid

• Nivell d'experiència---
• Tipus de contracteA temps complert
• Publicada30 de jul.

• Reference: AIPRETT24
• Start date: 30/07/2025 0:00:00
• Expiration Date: 08/08/2025 23:59:00
  
  

El Grupo de Telómeros y Telomerasa - Fundación Humanismo y Ciencia, dentro del Programa de Oncología Molecular, solicita candidatos/as para cubrir una plaza de Ayudante de Investigación Predoctoral para el diseño y ejecución de experimentos dirigidos a estudios del Microambiente tumoral en Glioblastoma Multiforme Mesenquimal y su relación con la proteína telomérica TRF1. Se va a estudiar el mecanismo de la proteína telomérica TRF1 en modelo de ratón con desarrollo de Glioblastoma Multiforme subtipo Mesenquimal. Específicamente, el estudio de TRF1 en el endotelio tumoral.

Selection Criteria

• Grado en Biotecnología. - Máster en Investigación en Biología Celular, Molecular y Genética. - 4 años de experiencia en investigación relacionada con telómeros, Glioblastoma y microambiente tumoral, concretamente endotelio, en modelos de ratón. - Experiencia en cirugía intracraneal. Requiere función A, B y C de manipulación de animales “Diseño de Proyectos y Procedimientos”. - Habilidades técnicas: Generación de modelos animales. Se valorará muy positivamente experiencia en cirugía intracraneal. Experiencia en cultivos celulares de células DF1, extracción de ADN/ARN, PCR estándar, qRT-PCR, qFISH, Western blot, técnicas de histología, microscopia confocal, análisis y procesamiento de imágenes.
  
  

The CNIO Offers

• Incorporación a un Centro de Investigación de relevancia internacional.
• Remuneración competitiva.
• Beneficios sociales.
• Contrato laboral asociado al proyecto.

• Nivell d'experiència---
• Tipus de contracteA temps complert
• Publicada30 de jul.

If you are a current Jazz employee please apply via the Internal Career site.

Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information.

Field-based role, 70% in field

Territory: Madrid, Seville and South of Spain

Position Overview

The Medical Science Liaison (MSL) will focus on identifying, developing and maintaining long-term collaborative partnerships with specified Key Opinion Leaders (KOLs) /External Clinical and Scientific Experts and assigned institutions to provide scientific and clinical trial support for future epilepsy portfolio. The MSL will serve as a primary liaison for clinical and scientific information exchange with KOLs/External Clinical and Scientific Experts and health care providers and will be leading discussions relating to therapeutic areas of importance to Jazz and the provision of scientific and medical data on both licensed and unlicensed Jazz products in response to appropriate requests from Healthcare Professionals (HCPs).

The MSL will be the primary conduit for Medical Affairs communications and interactions for their assigned institutions and organizations and will ensure effective communication across multifunctional teams in carrying out Medical Affairs projects.

Key Responsibilities/Accountabilities

External Stakeholders

Building Partnerships with HCPs

• Identifying national, regional and local KOLs in the area of Neurology & Rare Diseases, and developing and maintaining long-term collaborative relationships.
• Developing synergistic relationships with KOLs to expand research, advisory and educational partnership opportunities and developing synergistic scientific exchange opportunities between with internal and external colleagues.
• Delivering regional engagement plans with KOLs, based upon insights into their specialties and interests in specific areas of improving patient care.
• Engaging with specific Clinical and Scientific experts and Institutions/Organisations in the territory, through appropriate high-level scientific support for research activities, publications, education, consulting and other Medical Affairs initiatives.
• Understanding the needs of HCPs and developing insights through listening and observing the challenges faced in the treatment of serious diseases in paediatric and adult neurology therapy areas.
  
  

Providing Expertise in Jazz Medicines to Clinical Professionals, in a reactive environment

• Possess an in-depth knowledge of Jazz medicines, answering questions from HCPs, communicating salient facts in a clear, factual and non-promotional manner.
• Providing reactive medical support and scientific medical presentations within the therapeutic area to external stakeholders as needed.
• Becoming the ‘go to’ person for Clinician’s field of Rare Disease Neurology and cannabinoid therapies.
• Work with a diverse range of functions (e.g. Medical Information, Pharmacovigilance) to provide the optimal all-round medical service provision to partners.
  
  

Delivering on partnership projects, in a compliant therapy area environment

• Developing country medical projects in collaboration with HCPs (round table meetings, diagnosis workshops, rare disease forums, etc) within the defined therapeutic area.
• Providing medical support and International Congress, including lead, design and delivery of medical function activities, and working with commercial colleagues in the appropriate frameworks.
• Running appropriate advisory board panel meetings, to seek answers to questions specific to the needs and understanding of the Jazz Medical function business.
• Coordinating interactions with academic societies, research groups and other national organisations.
• Exploring novel educational opportunities with healthcare associations and ancillary healthcare professionals.
• Spending the majority of time in a field-based role, developing projects through self-motivation, and the identification of appropriate opportunities to help improve HCP education and patient care.
  
  

Working in a compliant environment, with patient safety and care at the heart of all activities

• Ensuring pharmacovigilance excellence, through adverse event reporting monitoring and liaising with HCPs to gather additional Drug Safety information as requested.
• Maintaining a strict delineation/definition with non-medical colleagues.
• Maintaining an understanding and application of local regulation in all activities.
  
  

Internal Functional Group Collaboration

Interfacing compliantly with commercial and marketing colleagues

• Participating in scientific and medical training of sales colleagues, and Jazz partner organisations.
• Responding to complex scientific enquires from the field, received through the commercial force. Providing scientific and medical support for internal meetings and projects as needed.
• Working within defined SOPs across functions for optimal team delivery for Jazz business.
  
  

Clinical Development and Studies

• Identifying and supporting Phase II-IV sites as required and working with the clinical team as major liaison for trial sites.
• Receiving and processing Investigator Initiated Trials (IIT) from the environment, and working with the medical and clinical team to ensure all IIT are providing appropriate support.
  
  

Leading the production of Medical Documents, Presentations, and Reports, working across a range of Jazz functions

• Identify, understand, distill and communicate new and complex data from inside Jazz and from the external environment.
• Produce educational materials, using various media, and lead on internal education and teaching activities within the environment of the EU medical team.
• Providing field updates regarding topics of interest for creation and/or updating of Standard Response Letters.
• Contribute to the National and International Medical team for development of Medical team ways of working, and aligned execution of the EU Medical strategy.
  
  

Others

• Communicating with all medical, research and development and commercial organisation as delineated by policies.
• Maintaining and continually developing scientific knowledge related to approved products and pipeline agents, and the relevant competitive landscape.
• Working within National and International Medical Environment, taking individually responsibility within with a large team ethos, to provide the best in class medical group.
• Operates in accordance with the Jazz corporate values of being patient driven, passionate, innovative, collaborative, accountable, having integrity and achieving excellence
• Works in accordance with the systems in place with regards to health & safety, security and the environment
  
  

Knowledge

KEY REQUIREMENTS

• Scientific Graduate with a higher qualification (e.g. PhD, Pharm D, MSc etc.)
  
  

Experience

• Proven track record of success in KOL management with an established network of contacts within the Pharmaceutical industry, and ability to build contacts, work in the field with external stakeholders.
• Significant Medical Science Liaison experience and strong knowledge of the pharma/biotech industry
• Experience in the therapy areas of epilepsy or neurology in general, is desirable.
• Clear understanding of MSL roles and responsibilities and Medical Affairs activities, including publication planning, medical information and advisory boards.
  
  

Skills

• Excellent interpersonal communication and relationship building skills.
• Strong multi-tasking, time management and organisational skills for a busy environment with a demonstrated ability to prioritise multiple assignments and deliver results while meeting deadlines.
• Demonstrated ability to lead and coordinate meetings.
• Demonstrated strong understanding of clinical research trial design.
• Excellent verbal, written communication and presentation skills. Ability to clearly articulate complex scientific concepts in one-to-one and group settings.
• Proactive approach with proven ability to take initiative and work both independently and as part of a team.
  
  

Attributes And Behaviours

• Proven track record in delivering on projects at the country level, with both internal and external stakeholders, also with the ability to manage partners and work with ‘dotted line’ matrix team flows.
• Strong organisational abilities, with an ability to prioritise tasks, and place the customer needs at the forefront of activities.
• Strong IT skills, with an ability to create informative and factual scientific documents and presentations, to distill complex data in a timely manner.
• Full understanding of the compliance environment and ability to design activities to fit within local regulatory framework and understanding of approval processes.
• Fluent in English and Spanish.
  
  

Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.

The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: https://careers.jazzpharma.com/benefits.html.

• Nivell d'experiència---
• Tipus de contracteA temps complert
• Publicada29 de jul.

Office

Job Description

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

Job Description

MSL Lead

Gilead has declared Oncology as one of the key therapeutic areas for future growth. Gilead is growing its pipeline in oncology through internal research, partnerships and acquisitions. We have an exciting opportunity to join the team to support the launch planning and execution for novel pipeline oncology products, across multiple tumor types and treatment settings.

This is a field-based Medical Scientist (MS) Lead position and will require national and international travel (including internal meetings and external scientific conferences) once travel restrictions are eased. The focus will be on the team delivering high quality scientific exchange with specialist hospital staff working in the field of Breast Cancer and other solid tumours. There will be opportunities for input into strategy and tactics, as well as other project work in addition to management of the team.

Responsibilities:

• Provides the MSs with a clear vision of the strategy and field goals and objectives in close alignment with the head office TA Lead and foster a collaborative team environment.
• Executes the strategy and regional/national Plan of Actions (POAs) in the field.
• Is responsible for ensuring successful scientific exchange about treatment landscape and therapeutic options with external stakeholders.
• Acts as the interface between the field and the office, ensuring field insights, local research initiatives and data generation are appropriately communicated and discussed within the organization at national and international level.
• Manages the planning of MS activities and ensures cross functional alignment within the Organization and that the MS team works collaboratively with Gilead personnel in Sales, Regional Market Access, Marketing, Clinical Research, Global Safety and Medical Communication.
• Conducts regular MS field visits with each team member.
• Ensures the MS team maintains excellent professional relationships through facilitation of their training and development with each having an individual development plan. Provide continuous constructive feedback (performance and personal development). Periodically meet with MS to conduct performance evaluations.
• Provide the MSs with projects and responsibilities to increase their visibility and boost their professional development.
  
  

Critical Competencies:

• The candidate must have a strong scientific background with a medical or pharmacy degree, preferably a higher (e.g. MSc or PhD) degree.
• Good knowledge of the Spanish healthcare environment and management of solid tumours (ideally breast cancer) is required. Knowledge of Portuguese and the health system would be an asset.
• Previous Medical Scientific Liaison management experience and as an MSL is highly preferable.
• The individual must have excellent communication, presentation and organizational skills.
• The ability to work well in a team, proactivity and personal initiative are key attributes as is a willingness to take ownership of and deliver specific projects.
  
  

Equal Employment Opportunity (EEO)

It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual’s gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.

For Current Gilead Employees And Contractors:

Please apply via the Internal Career Opportunities portal in Workday.

• Nivell d'experiència---
• Tipus de contracteA temps complert
• Publicada23 de jul.

ERP

Si tienes pasión por las ventas y quieres formar parte de una compañía internacional pionera en investigación, desarrollo y comercialización con un claro propósito de promover y mejorar la Salud Bucal de las personas ¡Sigue leyendo!

En esta posición vas a tener la oportunidad de trabajar como Visitador/a Médico/a para el área de Madrid (centro), rodeado de un gran equipo de profesionales. Buscamos personas motivadas y apasionadas con alta responsabilidad para desarrollar sus funciones.

Que te ofrecemos:

• En Dentaid te ofrecemos una posición para que te desarrolles como profesional en un equipo de trabajo multidisciplinario donde compartirás conocimiento y visiones con profesionales de diferentes especialidades.
• Número de días de vacaciones muy por encima de la media del sector.
• Retribución flexible.
• Descuento en productos Dentaid y demás descuentos en eventos y servicios por ser parte de nuestra empresa.
• Coche de empresa, teléfono móvil y tablet para uso profesional.

¿Cuál será tu misión?

La finalidad de la posición es la de situarnos como laboratorio referente de salud bucodental y poder conseguir los objetivos marcados.

¿Qué te hará tener éxito en esta posición?

• Formación preferentemente en Ciencias de la Salud (Biología, Química, Farmacia, Odontología, o similar).
• Valorable formación en área Comercial y Marketing.
• Carné de conducir en vigor.
• Experiencia previa de 2-3 años en las funciones descritas.
• Usuario/a habitual de herramientas CRM o ERP.
• Disponibilidad para viajar.
• Dotes de comunicación y negociación (escucha activa y elocuencia).
• Capacidad de planificación en base al análisis de datos.
• Orientación a la consecución de objetivos/resultados.
• Habilidad para entender objetivos comunes y trabajar en equipo.

Tus responsabilidades serán:

• Analizar rutas asignadas y preparar previamente cada visita para tener claro los objetivos de las mismas.
• Establecer planes de acción que permitan la consecución de los objetivos marcados.
• Visitar a los profesionales segmentados de la zona asignada.
• Presentar y argumentar las propiedades de los productos del portafolio a las clínicas para conseguir los acuerdos de receta.
• Dar seguimiento y soporte a incidencias de clientes.
• Cumplir las normas de gestión de residuos, con las buenas prácticas ambientales en su puesto de trabajo, así como cualquier otro requerimiento de la dirección i/o persona responsable del SIG con el fin de adecuar y cumplir con los requisitos legales y otros requisitos aplicables.
• Comunicar posibles mejoras ambientales a implantar o bien detección de irregularidades detectadas.

Dentaid es una compañía que vela por la igualdad de oportunidades y diversidad no siendo discriminatoria en raza, religión, nacionalidad, género, edad, diversidad funcional.

Si quieres tener la oportunidad de formar parte de una empresa de salud bucal, con central en Cerdanyola del Vallès, y filiales localizadas en Europa y Latinoamérica y cuyo propósito es promover y mejorar la salud bucal de las personas durante toda su vida, ¿a qué esperas?