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

Global Regulatory Scientist
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Grado
- Seguro dental
- Seguro oftalmológico
Artificial Intelligence Research Scientist
SpotLab —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Informática
Solicitud rápida
Medical Information Associate- Italian language
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Microsoft Word
- Microsoft Excel
- Servicio al cliente
Solicitud rápida
3d
Access Field Head
Novartis —Madrid, Madrid provincia
- De 109.800 € a 204.000 € al año
- Jornada completa
- Negociación
10d
Senior Statistician
PSI CRO —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Máster
Solicitud rápida
9d
Account Manager
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Ventas
- Servicio al cliente
- Grado
- Teletrabajo opcional
Senior Pharmacovigilance Officer, Team Lead/ Case Processing Manager- Medical Device experience needed
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Inglés
- Microsoft Office
- Gestión del tiempo
Solicitud rápida
Delegad@ Hospitalario - Madrid
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Habilidades organizativas
- Habilidades de comunicación
- Formación continua
Global Study Manager - Single Sponsor dedicated (in EMEA)
IQVIA —Madrid, Madrid provincia
- De 171.500 € a 404.600 € al año
- Jornada completa
- Inglés
- Investigación
- Máster
- Teletrabajo opcional
Risk Manager
Sinclair —San Fernando de Henares, Madrid provincia
- Trabajo híbrido
- Inglés
- Máster
Talent Acquisition Specialist EMEA
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Español
- Servicio al cliente
- Inglés
8d
Consultant – Global Advisory Services
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Máster
- Project management
Delegad@ EREP-Madrid
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
Principal Statistician (Pharmacokinetics)
PSI CRO —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
Solicitud rápida
Team Lead, eCOA project management
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Project management
- Seguro dental
- Seguro oftalmológico
4d
Market Access Director Oncology
Regeneron —Madrid, Madrid provincia
- De 96.000 € a 160.000 € al año
- Trabajo híbrido
- Grado
- Seguro dental
- Vacaciones pagadas
Associate Pharmacovigilance Project Director (Delivery)- Europe
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Project management
- Gestión de conflictos
- Liderazgo
Solicitud rápida
5d
Site Engagement Manager
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Grado
- Seguro dental
- Seguro oftalmológico
Senior Editor - The Lancet’s eBioMedicine
RELX —Madrid, Madrid provincia
- De 36.400 € a 63.600 € al año
- Jornada completa
- Doctorado
- Inglés
- Investigación
Senior Editor - The Lancet’s eBioMedicine
Elsevier —Madrid, Madrid provincia
- De 36.400 € a 63.600 € al año
- Jornada completa
- Doctorado
- Inglés
- Investigación

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

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Global Regulatory Scientist

ICON Plc -
Madrid, Madrid provincia

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Detalles del empleo

Jornada completa

Beneficios

Seguro dental
Seguro oftalmológico
Plan de pensiones

Cualificaciones

Grado

Descripción completa del empleo

Global Regulatory Scientist/Senior Global Regulatory Scientist

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Global Regulatory Scientist at ICON, you will prepare strategy and coordinate global clinical trial regulatory deliverables in compliance with ICON policies, applicable regulations, and ICH-GCP principles.

What You Will Do:

You will contribute to regulatory affairs activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:

Develop and implement global clinical trial submission strategies and regulatory plans in collaboration with stakeholders.
Prepare, review, and finalize core documentation and ensure compliance with regulatory requirements.
Coordinate submissions to regulatory agencies, ethics committees, and country-level authorities.
Track and report submission progress in ICON systems, ensuring accuracy and completeness of documentation.
Represent Regulatory during audits, CAPAs, and client meetings, providing strategic input and solutions.

Your Profile:

You will bring relevant regulatory affairs experience, along with the following qualifications and skills.

Required qualifications and experience:

Bachelor's degree and 0-3 years of relevant regulatory submission experience.
Strong understanding of ICH-GCP and global regulatory guidelines.
Excellent organizational and communication skills with attention to detail.
Willingness to travel as required (approximately 10%)

#LI-TK1

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request .

Are you a current ICON Employee?

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clinical research empleos en alcobendas, md

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Senior Pharmacovigilance Officer, Team Lead/ Case Processing Manager- Medical Device experience needed

Delegad@ Hospitalario - Madrid

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Risk Manager

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Consultant – Global Advisory Services

Delegad@ EREP-Madrid

Principal Statistician (Pharmacokinetics)

Team Lead, eCOA project management

Market Access Director Oncology

Associate Pharmacovigilance Project Director (Delivery)- Europe

Site Engagement Manager

Senior Editor - The Lancet’s eBioMedicine

Senior Editor - The Lancet’s eBioMedicine

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

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