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

Global Regulatory Scientist
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Grado
- Seguro dental
- Seguro oftalmológico
Director Business Development - Oncology
TFS HealthScience —Madrid, Madrid provincia
- Teletrabajo
- Español
- Ventas
- Inglés
Solicitud rápida
Business Development Representative (2026-026)
Circle Cardiovascular Imaging —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- CRM software
- Español
- Ventas
Solicitud rápida
Senior Global Marketing Specialist
Ormco —Madrid, Madrid provincia
- CRM software
- Ventas
- Marketing
- Seguro dental
- Vacaciones pagadas
Director, Medical Safety
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Liderazgo
- Teletrabajo opcional
Sr. QA Auditor, GCP/Computerized Systems
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Word
- Investigación
- Teletrabajo opcional
Manager –Global Advisory Services
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Oficina
- Máster
Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Grado
- Teletrabajo opcional
Decision Analytics Consultant
Roche —Madrid, Madrid provincia
- Jornada completa
- Español
- Microsoft Excel
- Informática
International Product Manager | Endodontics
Henry Schein España S.L. —Madrid, Madrid provincia
- 41.000 € al año
- Jornada completa
- Trabajo híbrido
- Español
- Marketing
- Inglés
National Sales Manager - Medical
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Microsoft Office
- Grado
Director, Site Start up
Precision Medicine Group —Madrid, Madrid provincia
- Teletrabajo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
3d
Data Architect
Roche —Madrid, Madrid provincia
- Jornada completa
- Azure
- Máster
- AWS
Medical Information Specialist with Dutch, French and English
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Grado
- Habilidades organizativas
- Teletrabajo opcional
R&D Engineer
Ormco —Madrid, Madrid provincia
- Doctorado
- Informática
- Inglés
- Seguro dental
- Vacaciones pagadas
RWD Analytics Engineer
Roche —Madrid, Madrid provincia
- Jornada completa
- Informática
- Inglés
- Máster
Director, Site Start up
Precision for Medicine —Madrid, Madrid provincia
- Teletrabajo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Solicitud rápida
3d
Principal Statistical Programmer - FSP (Permanent Homebased) m/w/d
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Informática
- Grado
- Teletrabajo opcional
Senior Director, Commercial Sales & Operations, Brand Outsourcing & HCP Engagement
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Ventas
- Liderazgo
Global Trial Delivery Lead - Sponsor Dedicated
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
- Teletrabajo opcional

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

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Global Regulatory Scientist

ICON Plc -
Madrid, Madrid provincia

Solicitar ahora

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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Refina tu búsqueda

clinical research empleos en la moraleja, md

Global Regulatory Scientist

Director Business Development - Oncology

Business Development Representative (2026-026)

Senior Global Marketing Specialist

Director, Medical Safety

Sr. QA Auditor, GCP/Computerized Systems

Manager –Global Advisory Services

Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)

Decision Analytics Consultant

International Product Manager | Endodontics

National Sales Manager - Medical

Director, Site Start up

Data Architect

Medical Information Specialist with Dutch, French and English

R&D Engineer

RWD Analytics Engineer

Director, Site Start up

Principal Statistical Programmer - FSP (Permanent Homebased) m/w/d

Senior Director, Commercial Sales & Operations, Brand Outsourcing & HCP Engagement

Global Trial Delivery Lead - Sponsor Dedicated

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

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