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

Global Regulatory Scientist
ICON Plc —Madrid, Madrid provincia
- Jornada completa
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Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)
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Ormco —Madrid, Madrid provincia
- Doctorado
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IQVIA —Madrid, Madrid provincia
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Roche —Madrid, Madrid provincia
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IQVIA —Madrid, Madrid provincia
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Roche —Madrid, Madrid provincia
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IQVIA —Madrid, Madrid provincia
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Quiero recibir la alerta de empleo más reciente de clinical research en tres cantos, 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 tres cantos, md

Global Regulatory Scientist

Database Operator (Dutch Speaker) Homebased Fixed-Term

Delegad@ E-Consent - Granada

Senior Global Marketing Specialist

Director, Medical Safety

Business Development Representative (2026-026)

Sr. QA Auditor, GCP/Computerized Systems

Global Team Leader - IVDR

Decision Analytics Consultant

International Product Manager | Endodontics

Manager –Global Advisory Services

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

Director, Site Start up

R&D Engineer

National Sales Manager - Medical

Data Architect

Medical Information Specialist with Dutch, French and English

Director, Site Start up

RWD Analytics Engineer

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

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

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