55 Ofertas de Astrazeneca en España

Overview

A postdoctoral position in HIV-1 RNA structural biology and antiviral drug discovery is available in the Laboratory of Structural and Computational Biochemistry led by José Gallego at Catholic University of Valencia (UCV). The postdoctoral associate will be engaged in a research project funded by the PROMETEO program of Generalitat Valenciana, Spain, and focused on the study of the conformational dynamics of the Rev Recognition Element (RRE) in the HIV-1 RNA and the discovery of antiviral small-molecule agents blocking the complex between this motif and the Rev protein.

Catholic University of Valencia

The selection process ends once a candidate is selected.

About Us:
We are a U.S.-based clinical research organization seeking a skilled and motivated Clinical Trials Recruiter to join our team.

Job Description:
As a Clinical Trials Recruiter, you will be responsible for writing and posting ads to attract qualified participants, reaching out to potential candidates, and conducting prescreening interviews to determine eligibility. You will maintain participant information accurately in our CRM, communicate clearly with candidates to address questions, and ensure they have a positive experience throughout the recruitment process. Additionally, you may be required to translate recruitment materials and participant communication between English and Spanish. You'll manage scheduling and coordinate with the clinical team to meet recruitment goals, adapting recruitment strategies as needed to maximize participant engagement.

Requirements:

• Fluency in both English and Spanish, with a minimum C1 level proficiency in spoken and written communication.
• At least 4 years of experience in clinical recruitment, sales, or customer support. Experience in the medical field or healthcare is a plus.
• Strong technical skills, with 2+ years of experience using CRM systems and proficiency in Microsoft Office Suite. Experience with ad-writing for recruitment is beneficial.
• Excellent interpersonal skills, with the ability to build rapport over the phone and communicate effectively with a diverse range of participants.

Benefits:

• Remote Work
• Competitive Pay in USD
• Enhance Your CV: Gain valuable experience by working for a U.S.-based company, adding a strong international credential to your resume.
• Professional Growth: Develop skills in clinical trials and participant engagement, expanding your knowledge of the clinical research field.

Who We Are
We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us

What a Clinical Trials Associate Does At Worldwide
As a Clinical Trials Associate, you are responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately.

What You Will Do

• Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
• Maintain and quality audit to ensure the most recent revisions of documents are on the project portals
• Assist the project team with the preparation and shipment of clinical trial documentation, including the Investigator Site File
• Maintain version and quality control of project documentation and submit to the trial master file
• Assist with the tracking and maintenance of project-related information, including site medical questions and answer logs

What You Will Bring To The Role

• Excellent written and verbal English as well as fluency of the language of the country of location
• Ability to handle multiple tasks and exercise independent judgment
• Strong attention to detail and focus on the quality of work
• Strong organizational and problem-solving skills
• Excellent skills in MS Office applications, including Outlook, Word, Excel, and PowerPoint

Your Experience

• Degree level qualification or equivalent experience plus a minimum of one years' experience in a related role
• Skill sets and proven performance equivalent to the above

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide For more information on Worldwide, visit or connect with us on LinkedIn.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We're on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law
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PSI CRO Madrid, Community of Madrid, Spain

PSI CRO Madrid, Community of Madrid, Spain

At PSI, the Proposal Manager coordinates all phases of PSI’s proposal process while maintaining the company’s win rate of 30% and higher. You will contribute to RFP strategy and bid defense materials. You will partner with global teams of subject matter experts from Feasibility, Medical Affairs, Project Management, Clinical Operations, Budgeting, and Business Development to rapidly produce winning proposals.

• Develop high-quality strategic proposals that meet clients’ needs
• Prepare viable RFP calendars and ensure RFP milestones are met by all involved individuals in a timely manner
• Organize, attend, and lead strategy calls for RFPs
• Develop draft budgets in CLARITY
• Contribute to study modeling in VISIONAL
• Review clients’ specifications and obtain quality feedback from stakeholders
• Work with the budgeting team to develop competitive final budgets
• Prepare vendor RFPs and obtain vendor quotes
• Provide support for bid defense meetings

• A minimum of a four-year degree from an accredited college or university
• Experience managing full-service clinical trial proposals at a CRO
• Writing and editing skills
• Analytical skills
• Time management and organization skills
• Flexibility and creativity in responding to potential clients
• Proficiency in Microsoft Word, Excel and PowerPoint

This is a creative, tight-knit team of professionals motivated by producing quality proposals that resonate with our customers. Our culture is open, collaborative, and purposeful. We’re looking for talented people who value tailored proposals over templates.

PSI is a leading Contract Research Organization (CRO) with about 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.

At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.

We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.

At PSI, Proposal Manager coordinates all phases of PSI’s proposal process while maintaining the company’s win rate of 30% and higher. You will contribute to everything from RFP strategy to bid defense slide decks. You will partner with global teams of subject matter experts from Feasibility, Medical Affairs, Project Management, Clinical Operations, Budgeting, and Business Development to rapidly produce winning proposals.

This proposal development will include:

• Developing high-quality strategic proposals thatmeet our clients’ needs
• Preparing viable RFP calendars and ensuring RFP milestones are met by all involved individuals in a timely manner
• Organizing, attending, and leading strategy calls for RFPs
• Developing draft budgets in CLARITY
• Contributing to study modeling in VISIONAL
• Reviewing clients’ specifications, obtaining quality feedback from various stakeholders within the company
• Working with the budgeting team to develop competitive final budgets
• Preparing vendor RFPs and obtaining vendor quotes
• Providing support for bid defense meetings

• A minimum of a four-year degree from an accredited college or University
• Experience managing full-service clinical trial proposals at a CRO is a must
• Writing and editing skills
• Analytical skills
• Time management and organization skills
• Flexibility and creativity in responding to potential clients
• Proficiency in Microsoft Word, Excel and PowerPoint

This is a creative tight-knit team of professionals motivated by producing quality proposals that resonate with our customers. Our culture is open, collaborative, and purposeful. We’re now looking for talented people who don’t believe in one-size-fits-all templates and have a passion for writing proposals that get read and remembered.

Overview

Leading multinational company in the dermocosmetic sector, headquartered in Barcelona and present in over 50 countries, is looking to add a DermoLab Technician to its team.

• Carry out efficacy tests prior to the production of the finished product.
• Carrying out work and equipment follow-up protocols.
• Elaboration and drafting of SOPs (Standard Operating Procedures).
• Receive support from Medical Marketing to know the protocols to follow.
• Carry out in vivo studies.
• Collaboration in internal sensory tests.
• Management of volunteer panel.

• Education : Degree in Chemistry, Pharmacy, Biology or similar. Notions of statistics to interpret data.
• Experience : 1-2 years of experience in a similar position.
• Languages : Spanish & English High Level (C1)

Alliance Healthcare España

Alliance Healthcare España es uno de los líderes en la distribución farmacéutica en el mercado español. Presente en todo el país con 12 centros de distribución y un equipo comprometido de profesionales. Forma parte de Cencora, una empresa global de referencia en el sector farmacéutico.

Descripción del Puesto:

Actualmente, estamos en búsqueda de un/a Project Manager para unirse a nuestro equipo en Viladecans, Barcelona. Esta es una oportunidad muy interesante para liderar proyectos logísticos en el ámbito de los ensayos clínicos.

Liderazgo de Proyectos: Dirigir y gestionar proyectos logísticos de ensayos clínicos, asegurando el cumplimiento de plazos y objetivos.

Coordinación Interdepartamental: Colaborar con los equipos de Business Development, Dirección Técnica, Supply Chain y Operaciones para garantizar el éxito del proyecto.

Comunicación Interna: Facilitar la comunicación sobre tareas y responsabilidades entre el equipo de Operaciones y otros departamentos involucrados.

Supervisión de Procesos: Monitorear el desarrollo adecuado de los procesos junto con el equipo interno, asegurando la calidad y el cumplimiento de los estándares.

Diseño de Procedimientos: Crear o mejorar procedimientos para resolver desafíos y necesidades, así como para implementar nuevos servicios a lo largo del proyecto.

Relación con Clientes: Mantener comunicación fluida con los clientes a través de reuniones y teleconferencias, asegurando su satisfacción y abordando inquietudes.

Reporting: Elaborar informes detallados sobre el progreso y las actividades del proyecto.

Coordinación Nacional e Internacional: Participar activamente en la coordinación de ensayos clínicos a nivel nacional e internacional, asegurando la alineación de objetivos y procesos.

Conocimientos y Experiencia:

Experiencia: Mínimo 4 años de experiencia como Project Manager, preferiblemente de proyectos donde se haya tenido contacto con un cliente externo.

Formación: Título en Ingeniería, Ciencias de la Salud o áreas relacionadas.

Inglés: Nivel alto imprescindible, se realizará una prueba durante el proceso de selección.

Habilidades Personales: Persona organizada, proactiva y con habilidades para trabajar en equipo.

Herramientas Informáticas: Dominio de Microsoft Office y Microsoft Project a nivel usuario, así como experiencia en sistemas informáticos de gestión.

Integración en un grupo con presencia global y amplias oportunidades de desarrollo profesional.

Plan retributivo flexible.

Ubicación: Viladecans.

Opción de smartworking 2 días a la semana.

Flexibilidad horaria de entrada y salida, con viernes intensivo.

Descuentos exclusivos en productos de la empresa (parafarmacia, cosméticos, etc.).

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!

Alliance Healthcare España

Alliance Healthcare España es uno de los líderes en la distribución farmacéutica en el mercado español. Presente en todo el país con 12 centros de distribución y un equipo comprometido de profesionales. Forma parte de Cencora, una empresa global de referencia en el sector farmacéutico.

Descripción del Puesto:

Actualmente, estamos en búsqueda de un/a Project Manager para unirse a nuestro equipo en Viladecans, Barcelona. Esta es una oportunidad muy interesante para liderar proyectos logísticos en el ámbito de los ensayos clínicos.

Responsabilidades:

• Liderazgo de Proyectos: Dirigir y gestionar proyectos logísticos de ensayos clínicos, asegurando el cumplimiento de plazos y objetivos.

• Coordinación Interdepartamental: Colaborar con los equipos de Business Development, Dirección Técnica, Supply Chain y Operaciones para garantizar el éxito del proyecto.

• Comunicación Interna: Facilitar la comunicación sobre tareas y responsabilidades entre el equipo de Operaciones y otros departamentos involucrados.

• Supervisión de Procesos: Monitorear el desarrollo adecuado de los procesos junto con el equipo interno, asegurando la calidad y el cumplimiento de los estándares.

• Diseño de Procedimientos: Crear o mejorar procedimientos para resolver desafíos y necesidades, así como para implementar nuevos servicios a lo largo del proyecto.

• Relación con Clientes: Mantener comunicación fluida con los clientes a través de reuniones y teleconferencias, asegurando su satisfacción y abordando inquietudes.

• Reporting: Elaborar informes detallados sobre el progreso y las actividades del proyecto.

• Coordinación Nacional e Internacional: Participar activamente en la coordinación de ensayos clínicos a nivel nacional e internacional, asegurando la alineación de objetivos y procesos.

.

Conocimientos y Experiencia:

• Experiencia: Mínimo 4 años de experiencia como Project Manager, preferiblemente de proyectos donde se haya tenido contacto con un cliente externo.

• Formación: Título en Ingeniería, Ciencias de la Salud o áreas relacionadas.

• Inglés: Nivel alto imprescindible, se realizará una prueba durante el proceso de selección.

• Habilidades Personales: Persona organizada, proactiva y con habilidades para trabajar en equipo.

• Herramientas Informáticas: Dominio de Microsoft Office y Microsoft Project a nivel usuario, así como experiencia en sistemas informáticos de gestión.

¿Qué Te Ofrecemos?

• Integración en un grupo con presencia global y amplias oportunidades de desarrollo profesional.

• Contrato indefinido.

• Plan retributivo flexible.

• Ubicación: Viladecans.

• Opción de smartworking 2 días a la semana.

• Flexibilidad horaria de entrada y salida, con viernes intensivo.

• Programas de formación online.

• Descuentos exclusivos en productos de la empresa (parafarmacia, cosméticos, etc.).

Benefit offerings outside the US may vary by country and will be aligned to local market practice. The eligibility and effective date may differ for some benefits and for team members covered under collective bargaining agreements.

Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law.

The company’s continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory.

Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call or email . We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned

Job Title : Proposal Manager

The successful candidate will be responsible for the preparation of technical and commercial proposals focused on the Power Market.

The proponent will analyze client invitation to bid requirements, evaluate market technologies, lead internal tender preparations, and coordinate with construction management and partners to obtain bids from subcontractors.

The candidate will also supervise and monitor the accomplishment of the offer's estimate budget, prepare commercial and administrative documentation, and ensure the technical documentation is complete and adequate.

Additionally, the Proposal Manager will track and close the offer, prepare subsequent clarifications and amendments, and actively participate in negotiations with the Client.

• Analyze the Client's invitation to bid requirements and assure its completion.
• Evaluation of market technologies aiming for the main OEMs selection for a proposal.
• Lead the internal preparation of tenders, coordinating the different departments involved (technicians, procurement, legal, fiscal, estimates, etc.) to obtain the necessary information for the bid.
• Address and obtain clarifications from the Client.
• Coordinate with the Construction Management the construction strategy and the attainment of bids from subcontractors.
• Coordinate with partners, OEMs and / or subcontractors their correct involvement in the preparation of the technical and commercial proposal.
• Supervise and monitor the accomplishment of the offer's estimate budget.
• Prepare the commercial and administrative documentation, as well as assuring that the technical documentation is complete and adequate.
• Responsible for the correct emission of the technical-commercial proposal.
• Tracking and closing of the offer;
  
  prepare the subsequent clarifications and amendments to the presentation of the Offer.
• Actively participating in the negotiations with the Client.

PSI is a leading Contract Research Organization (CRO) with about 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.

At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.

We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.

At PSI, Proposal Manager coordinates all phases of PSI’s proposal process while maintaining the company’s win rate of 30% and higher. You will contribute to everything from RFP strategy to bid defense slide decks. You will partner with global teams of subject matter experts from Feasibility, Medical Affairs, Project Management, Clinical Operations, Budgeting, and Business Development to rapidly produce winning proposals.

This proposal development will include:

• Developing high-quality strategic proposals thatmeet our clients’ needs
• Preparing viable RFP calendars and ensuring RFP milestones are met by all involved individuals in a timely manner
• Organizing, attending, and leading strategy calls for RFPs
• Developing draft budgets in CLARITY
• Contributing to study modeling in VISIONAL
• Reviewing clients’ specifications, obtaining quality feedback from various stakeholders within the company
• Working with the budgeting team to develop competitive final budgets
• Preparing vendor RFPs and obtaining vendor quotes
• Providing support for bid defense meetings

• A minimum of a four-year degree from an accredited college or University
• Experience managing full-service clinical trial proposals at a CRO is a must
• Writing and editing skills
• Analytical skills
• Time management and organization skills
• Flexibility and creativity in responding to potential clients
• Proficiency in Microsoft Word, Excel and PowerPoint

This is a creative tight-knit team of professionals motivated by producing quality proposals that resonate with our customers. Our culture is open, collaborative, and purposeful. We’re now looking for talented people who don’t believe in one-size-fits-all templates and have a passion for writing proposals that get read and remembered.