Ofertas de empleo de Médico/a en Barcelona

• Flexibilidad horariaSí
• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada27 abr.

ASINSA SERVICIOS SANITARIOS busca un/a MÉDICO/A VISITAS DOMICILIARIAS

Asinsa, empresa lider desde hace 35 años en prestación de servicios sanitarios. Con sede en Barcelona capital trabajamos en varios sectores de sanidad privada: especialidades médicas en nuestro centro, reconocimientos de salud laboral y visitas de asistencia médica domiciliaria. Actualmente contamos con un equipo estable de más de 35 profesionales sanitarios, realizando diferentes turnos y horarios con mucha flexibilidad horaria.

Tareas

¿Qué ofrecemos?

-Contrato laboral indefinido.

-20 o 40 horas semanales repartidas en guardias

-Salario bruto anual: Base convenio+Pluses visitas realizadas+ Productividad (Aprox. 25.000€ para el contrato de 20h/ 50.000€ para el contrato de 40h)

-Gastos Km a cargo de la empresa

Horarios

-Flexibilidad horaria:

*Turnos de 7 a 15h y/o de 15 a 23h a repartir en guardias con otros compañeros

*Turnos de 21 a 07h a repartir en guardias con otros compañeros (plus nocturnidad)

-Incorporación inmediata

Requisitos

Imprescindible:

-carnet de conducir

-título homologado

-permiso de trabajo vigente

Beneficios

-Especial flexibilidad horaria

-Pluses por incentivos

-Posibilidad de vehículo de empresa (se valorará especialmente vehícuo propio))

• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada27 abr.

Teletrabajo Spark

Every 30 minutes, a stroke patient who could have been saved either dies or is permanently disabled because they were treated in the wrong hospital.

Our mission is clear: to increase the number of patients treated in stroke-ready hospitals and to optimize the quality of treatment in all existing stroke centers. We are building a global community of stroke centers and stroke-ready hospitals, working tirelessly to improve the quality of treatment for every stroke patient.

This is a unique opportunity to join IQVIA to enhance stroke care worldwide through a corporate social responsibility project.

We are seeking an Consultant in Barcelona, Spain, who will join an exciting working environment in a dynamic and international atmosphere.

Responsibilities:

After comprehensive and ongoing training, you will be ready to:

• Enhance the efficiency of stroke patient management
• Support hospitals and healthcare professionals with continuous training and organizational tools
• Serve as an expert Therapeutic Consultant, promoting new diagnostic and treatment guidelines to hospitals
• Foster and promote quality monitoring programs to ensure consistent hospital performance
• Expand the project's reach to new hospitals
• Lead multidisciplinary stroke teams through continuous improvement
• Improve therapeutic protocols in major hospitals
  
  

Required Skills:

• Excellent scientific background, ideally with a PhD in Neuroscience
• High motivation and strong interpersonal skills
• Fluency in English and Spanish
• Leadership abilities
• Proactive, flexible, and strong problem-solving skills
• Availability to travel up to 70% of the time
• Eligibility to work full-time
  
  

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes.

• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada26 abr.

About This Role

TFS HealthScience is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and functional service (FSP) solutions.

Medical Writer / Senior Medical Writer

The Scientific Medical Writer will support the development of scientific content creation:

• Medical Information Support: Production of new global standard scientific response content
• Publications Support: Production of abstracts, posters, manuscripts...
• Other scientific content: Scientific slide decks, Q&As, study summaries...
  
  

The Medical Writer will work under the guidance of the Corporate Therapeutic Areas in regard to content and timelines and adhere to defined company standards as well as safeguard that processes and system standards are followed.

Main activities

• Production of scientific content
• Update of existing content
• Adjust content according to the feedback received during review cycles.
• Obtain final approval from the relevant stakeholders
• Perform peer reviews for style and accuracy and for continuous improvement purposes.
  
  

Qualifications

Experienced Medical Writer (2 -5 years), with a scientific background and degree (PharmD, MD, PhD or Masters), at least 2-3 years developing high quality scientific medical/ content for pharma or an agency (quality reviewer)

Experience in writing and managing scientific publications (manuscripts, posters, abstracts, etc.).

Excellent medical writing skills. Strong attention to detail and accuracy, ability to manage and prioritize multiple, detailed activities, results-orientated with fast and focused execution.

Good communication, coordination and time management skills. Fluent in oral and written English with high level of communication skills.

Prior experience working in any of the therapeutic areas of Cardiovascular, Metabolism, Respiratory (CMR), Inflammation, Immunology, Retinopathy, Central Nervous System, and Oncology would be advantageous.

What We Offer

We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients

A Bit More About Us

Our journey began over 27 years ago in Sweden, in the city of Lund. As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working towards a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

Our core values of Trust, Quality, Passion, Flexibility, and Sustainability are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.

• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada25 abr.

Teletrabajo Agile Excel LESS PowerPoint Word

Description

Senior Medical Writer

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:

WORK HERE MATTERS EVERYWHERE

Why Syneos Health

• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.
  
  

Job Responsibilities

• Mentors and leads less experienced medical writers on complex projects, as necessary.
• Acts as lead for assigned writing projects.
• Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision.
• Develops or supports a variety of documents that include, but not limited to:
• Clinical study protocols and clinical protocol amendments;
• Clinical study reports;
• Patient narratives;
• Clinical development plans;
• IND submissions and annual reports;
• Integrated summary reports;
• NDA and (e)CTD submissions;
• Investigator brochures, as well as;
• Clinical journal manuscripts, clinical journal abstracts, and client presentations.
• Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or escalation as appropriate.
• Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency.
• Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables.
• Serves as peer reviewer on internal review team providing review comments on draft and final documents.
• Adheres to established regulatory standards, including but not limited to ICH-E3 guidelines, as well as Company Standard Operating Procedures, client standards, and Company and/or client approved templates when completing medical writing projects, on-time and on-budget.
• Performs on-line clinical literature searches, as applicable.
• Maintains familiarity with current industry practices and regulatory requirements and guidelines that affect medical writing.
• Maintains awareness of budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership.
• Completes required administrated tasks within the specified timeframes.
• Performs other work-related duties as assigned. Minimal travel may be required (less than 25%).
  

Qualifications

What we’re looking for

• Bachelor of Science degree with relevant writing experience or Bachelor of Arts degree (Social Sciences, English or Communications, preferred) with relevant scientific and/or medical knowledge and expertise.
• Extensive knowledge of English grammar and FDA and ICH regulations and guidelines as well as a familiarity with AMA style guide.
• Demonstrated high degree of independence with effective presentation, proofreading, interpersonal, and leadership skills and ensure a team-oriented approach.
• Strong proficiency in Word, Excel, PowerPoint, email, and Internet.
• Ability to demonstrate a familiarity with principles of clinical research and to interpret and present clinical data and other complex information.
  
  

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.

The annual base salary for this position ranges from $60,930.00 to $115,100.00 (US Only). The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada22 abr.

El Colegio pone a tu disposición un servicio de Información de Ofertas de Empleo Médico.En esta sección dispones de ofertas laborales específicas y permanentemente actualizadas.Jefe/a de la Unidad de Cuidados Intensivos - Centro Médico Teknon Estado:Tipo de contrato: IndefinidoSalario:Ubicación: (Municipio, provincia, etc...)Descripción del puesto: Jefe/a de la Unidad de Cuidados Intensivos en Centro Médico Teknon.En este rol, serás responsable de liderar y supervisar el equipo de la UCI, garantizando la atención de alta calidad a los pacientes críticos.

Tu labor será fundamental para mantener los estándares de excelencia y contribuir al bienestar de nuestros pacientes.Reportando directamente a la dirección médica, tendrás la oportunidad de trabajar en un entorno innovador y colaborativo, donde tu experiencia y liderazgo marcarán la diferencia en la vida de quienes más lo necesitan.Responsabilidades: Supervisar el personal de la UCI y coordinar las actividades diarias.Garantizar la calidad de la atención médica y el cumplimiento de protocolos.Participar en la formación y desarrollo del equipo.Colaborar en la toma de decisiones estratégicas para la mejora continua del servicio.Estudios requeridos: Titulación en Medicina y especialidad en Medicina Intensiva.Experiencia necesaria: Experiencia previa en posiciones de liderazgo en unidades de cuidados intensivos.Requisitos del puesto: Conocimientos sólidos en gestión de equipos y procesos clínicos.Capacidad para trabajar bajo presión y tomar decisiones acertadas en situaciones críticas.Excelentes habilidades de comunicación y trabajo en equipo.Orientación a la mejora continua y la excelencia en la atención al paciente.Beneficios: Oportunidad de crecimiento profesional en un centro médico de renombre.Trabajar con un equipo multidisciplinario altamente calificado.Paquete salarial competitivo y beneficios adicionales.Ambiente de trabajo estimulante y orientado a la excelencia.Colegio Oficial de Médicos de la Provincia de ValladolidC/ Pasión, 13, 3- 47001 Valladolid | Email: ****** - 983 355 488 - 983 351 703 | Fax - 983 350 254#J-18808-Ljbffr

• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada20 abr.

MerIT, consultoría de Recursos Humanos, está buscando cubrir la siguiente vacante:Reconocida empresa de Prevención de la Salud, con sede en Valladolid, necesita incorporar a su plantilla un Médico Especialista en Medicina del Trabajo (MIR).Funciones:1.

Exámenes de Salud en sede, y en ocasiones en empresas clientes; 2.

Validación de expedientes médicos.Muy valorable vehículo propio (desplazamientos ocasionales, dentro del horario de trabajo, se paga kilometraje).Contrato indefinido, y jornada intensiva de mañana.Interesados contactar a ******; O al teléfono: 647488667.#J-18808-Ljbffr