20 publicaciones de empleo destacadas de clinical research en la moraleja, md (¡Están contratando!)

Regulatory Intelligence - Offering Management (Pharma)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Microsoft Powerpoint
- Microsoft Excel
- Inglés
Global Regulatory Scientist
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Grado
- Seguro dental
- Seguro oftalmológico
PV Officer (experience in Medical devices required)
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Inglés
- Gestión del tiempo
Solicitud rápida
6h
Regulatory & Quality Lead – AI IVD Diagnostics
SpotLab —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Español
- Inglés
- Bachillerato
Solicitud rápida
Medical Safety Director, Clinical Scientist
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Teletrabajo opcional
4d
Senior Medical Writer - Early Phase (Single Sponsor Support)
Syneos - Clinical and Corporate - Prod —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
Senior Clinical Trial Manager - Internal Medicine
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Grado
- Liderazgo
- Seguro dental
- Seguro oftalmológico
Associate Medical Director- Neurology
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
Associate Pharmacovigilance Project Manager (Europe)
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Project management
- Liderazgo
Solicitud rápida
Senior Director, Drug Development
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Investigación
- Teletrabajo opcional
Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
Medical Information Associate- Italian language
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Microsoft Word
- Microsoft Excel
- Servicio al cliente
Solicitud rápida
5d
Senior Medical Information Associate Italian Language
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Servicio al cliente
- Inglés
- Habilidades de comunicación
Solicitud rápida
Delegado Derma y Estética - Madrid
IQVIA —Madrid, Madrid provincia
- 30.000 € al año
- Jornada completa
- Habilidades de comunicación
- Enfermería
Senior Site Contract Associate - IQVIA Biotech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Microsoft Office
- Grado
- Teletrabajo opcional
Product Data Officer - Medical Devicer (Fixed-Term Contract)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
10d
Compliance - Senior Consultant (Life Science exp mandatory)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Máster
- Grado
Delegad@ Hospitalario - Madrid
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Habilidades organizativas
- Habilidades de comunicación
- Formación continua
CRA I-II in Madrid. Sponsor dedicated.
サイネオス・ヘルス —Madrid, Madrid provincia
- Grado
11d
Senior Director / Executive Director Medical Writing
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Liderazgo
Solicitud rápida

Quiero recibir la alerta de empleo más reciente de clinical research en la moraleja, md

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Regulatory Intelligence - Offering Management (Pharma)

IQVIA -
Madrid, Madrid provincia

Solicitar ahora

Detalles del empleo

Jornada completa

Cualificaciones

Microsoft Powerpoint
Microsoft Excel
Inglés
Project management

Descripción completa del empleo

Madrid, Spain | Full time | Hybrid | R1540947

We are looking for a new team member to join in our Regulatory Offering Management Team the development, enhancement, and launch of Regulatory Intelligence solutions for the pharmaceutical industry. This role will work closely with cross-functional and international teams to drive offering strategy, market readiness, and customer value.

Key Responsibilities:

Support the development and commercialization of new Regulatory Intelligence offerings.

Collaborate with product, regulatory, marketing, and business stakeholders to deliver new solutions and enhancements.

Develop and maintain go-to-market materials, value propositions, and internal enablement resources.

Monitor regulatory trends, customer needs, and market developments to identify growth opportunities.

Manage multiple projects simultaneously, ensuring timely execution and alignment with business objectives.

Support stakeholder communication and drive cross-functional collaboration throughout the offering lifecycle.

Contribute to innovation initiatives, including the adoption of AI-enabled capabilities and solutions.

Required Qualifications:

Experience in Regulatory Affairs, Regulatory Intelligence, Life Sciences, or a related pharmaceutical field.

Strong understanding of regulatory processes and the needs of regulatory clients.

Excellent project management and organizational skills.

Strong written and verbal communication abilities.

Advanced proficiency in Microsoft PowerPoint and Excel.

Ability to work effectively in a global, cross-functional environment.

Strong attention to detail, problem-solving skills, and a proactive mindset.

Interest in digital transformation, innovation, and AI applications.

Preferred Qualifications:

Experience supporting product, offering, or solution development initiatives.

Advanced English level is required (at least C1)

Knowledge of go-to-market planning and commercialization activities.

Experience working with international teams and stakeholders.

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.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Where you'll work

Hybrid

You’ll split your time between home and the office, giving you the flexibility to focus where you work best while still building strong in-person connections with your team. This model combines the autonomy of remote work with the collaboration, energy and resources of an office environment.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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Refina tu búsqueda

clinical research empleos en la moraleja, md

Regulatory Intelligence - Offering Management (Pharma)

Global Regulatory Scientist

PV Officer (experience in Medical devices required)

Regulatory & Quality Lead – AI IVD Diagnostics

Medical Safety Director, Clinical Scientist

Senior Medical Writer - Early Phase (Single Sponsor Support)

Senior Clinical Trial Manager - Internal Medicine

Associate Medical Director- Neurology

Associate Pharmacovigilance Project Manager (Europe)

Senior Director, Drug Development

Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience

Medical Information Associate- Italian language

Senior Medical Information Associate Italian Language

Delegado Derma y Estética - Madrid

Senior Site Contract Associate - IQVIA Biotech

Product Data Officer - Medical Devicer (Fixed-Term Contract)

Compliance - Senior Consultant (Life Science exp mandatory)

Delegad@ Hospitalario - Madrid

CRA I-II in Madrid. Sponsor dedicated.

Senior Director / Executive Director Medical Writing

Quiero recibir la alerta de empleo más reciente de clinical research en la moraleja, md

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