20 publicaciones de empleo destacadas de clinical research en comunidad de madrid (¡Están contratando!)

Global Regulatory Scientist
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Grado
- Seguro dental
- Seguro oftalmológico
Senior Clinical Trial Manager - Internal Medicine
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Grado
- Liderazgo
- Seguro dental
- Seguro oftalmológico
CRA I-II in Madrid. Sponsor dedicated.
サイネオス・ヘルス —Madrid, Madrid provincia
- Grado
9d
Software Engineer for Healthcare Sector Projects
GMV —Tres Cantos, Madrid provincia
- Trabajo híbrido
- Seguro dental
Business Development Manager – Medical Affairs Solutions (IQVIA Pharma Review)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Desarrollo de negocios
CRA
Servier —Madrid, Madrid provincia
- Español
- Inglés
- Negociación
Medical Monitor (Gastroenterology)
PSI CRO —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Investigación
- Microsoft Office
Solicitud rápida
Core Information Offering Specialist - MedTech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Inglés
- Teletrabajo opcional
2d
Field Service Engineer - Diagnostics & Life Science
Revvity —Tres Cantos, Madrid provincia
- Español
- Inglés
- Sistema operativo Windows
- Seguro de vida
Associate Medical Director- Neurology
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
Senior Director, Drug Development
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Investigación
- Teletrabajo opcional
Senior Medical Writer - Early Phase (Single Sponsor Support)
Syneos - Clinical and Corporate - Prod —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
Medical Safety Director, Clinical Scientist
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Teletrabajo opcional
2d
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
Senior Site Contract Associate - IQVIA Biotech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Microsoft Office
- Grado
- Teletrabajo opcional
Associate Pharmacovigilance Project Director (Delivery)- Europe
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Project management
- Gestión de conflictos
- Liderazgo
Solicitud rápida
5d
Study Start Up Associate II
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Seguro dental
- Seguro oftalmológico
12d
Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
Sr Medical Project Manager
Gilead Sciences —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Inglés
9d
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 comunidad de madrid

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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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clinical research empleos en comunidad de madrid

Global Regulatory Scientist

Senior Clinical Trial Manager - Internal Medicine

CRA I-II in Madrid. Sponsor dedicated.

Software Engineer for Healthcare Sector Projects

Business Development Manager – Medical Affairs Solutions (IQVIA Pharma Review)

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Medical Monitor (Gastroenterology)

Core Information Offering Specialist - MedTech

Field Service Engineer - Diagnostics & Life Science

Associate Medical Director- Neurology

Senior Director, Drug Development

Senior Medical Writer - Early Phase (Single Sponsor Support)

Medical Safety Director, Clinical Scientist

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

Senior Site Contract Associate - IQVIA Biotech

Associate Pharmacovigilance Project Director (Delivery)- Europe

Study Start Up Associate II

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

Sr Medical Project Manager

Senior Director / Executive Director Medical Writing

Quiero recibir la alerta de empleo más reciente de clinical research en comunidad de madrid

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