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

Regulatory & Quality Lead – AI IVD Diagnostics
SpotLab —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Español
- Inglés
- Bachillerato
Solicitud rápida
Delegado Derma y Estética - Madrid
IQVIA —Madrid, Madrid provincia
- 30.000 € al año
- Jornada completa
- Habilidades de comunicación
- Enfermería
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
Senior Medical Information Associate Italian Language
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Servicio al cliente
- Inglés
- Habilidades de comunicación
Solicitud rápida
CRA I-II in Madrid. Sponsor dedicated.
サイネオス・ヘルス —Madrid, Madrid provincia
- Grado
10d
Senior Site Contract Associate - IQVIA Biotech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Microsoft Office
- Grado
- Teletrabajo opcional
Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
Senior Statistician
PSI CRO —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Máster
Solicitud rápida
9d
Senior Director / Executive Director Medical Writing
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Liderazgo
Solicitud rápida
Medical Information Associate- Italian language
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Microsoft Word
- Microsoft Excel
- Servicio al cliente
Solicitud rápida
3d
Artificial Intelligence Research Scientist
SpotLab —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Informática
Solicitud rápida
Access Field Head
Novartis —Madrid, Madrid provincia
- De 109.800 € a 204.000 € al año
- Jornada completa
- Negociación
10d
Compliance - Senior Consultant (Life Science exp mandatory)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Máster
- Grado
Medical Safety Director, Clinical Scientist
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Teletrabajo opcional
2d
Sr Medical Project Manager
Gilead Sciences —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Inglés
9d
Product Data Officer - Medical Devicer (Fixed-Term Contract)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
8d
Core Information Offering Specialist - MedTech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Inglés
- Teletrabajo opcional
3d
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

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Regulatory & Quality Lead – AI IVD Diagnostics

SpotLab -
Madrid, Madrid provincia

Solicitud rápida

Detalles del empleo

Jornada completa

Cualificaciones

ESO
Español
Inglés
Bachillerato
Grado
Farmacia
Inteligencia artificial

Descripción completa del empleo

We are facing a real challenge and looking for the right person to join our adventure.

SpotLab is a frontier AI laboratory dedicated to advancing biopharmaceutical research and diagnostic innovation through reliable and cutting-edge AI solutions. As a growing startup developing AI products for medical diagnosis, we need someone who can help us streamline processes and navigate regulatory changes to ensure compliance.

SpotLab has built a solid foundation in quality and regulatory affairs, including: the In Vitro Medical Device Manufacturer License granted by the Spanish Medicines Agency, a Quality Management System following ISO 13485 standards, CE Marking for two AI diagnostic products under the IVDD, and ISO 27001 certification. Now, we need to continue evolving our approach for the dynamic regulatory landscape.

This role offers a meaningful mission: you will help certify AI models for microscopy images in hematology and infectious diseases —pioneering a new era with real impact on patients' lives worldwide.

We have received more than 10 international awards, including the Seal of Excellence of the European Union. We are a multidisciplinary team with gender parity where engineers, doctors, clinical researchers, business managers, and others with diverse professional backgrounds complement each other.

Key Responsabilities:

Lead the CE marking plan and execution to certify AI-based IVD diagnostic products.
Act as the company’s PRRC (Person Responsible for Regulatory Compliance) for IVD products.
Own IVDR regulatory strategy and align product roadmap, evidence, and documentation to regulatory timelines.
Evolve and maintain a scalable QMS (ISO 13485-aligned).
Drive technical documentation and conformity assessment readiness.
Implement risk management and PMS/vigilance processes.
Coordinate with notified bodies and authorities.
Work with AI/engineering to ensure compliance with EU AI Act obligations.
Support regulatory audits, internal audits, and supplier evaluation meetings

Experience in SaMD (Software as a Medical Device) regulatory frameworks and compliance activities.
Experience with EU medical device regulations, including IVDR (EU) 2017/746 and/or MDR (EU) 2017/745.
Understanding of emerging AI regulations in healthcare, including the EU AI Act, and the ability to translate them into practical compliance actions.
Proven ability to interpret and apply regulatory requirements specifically for AI-based systems in the medical sector.
Excellent analytical skills, with strong attention to detail and clear, structured communication (written and verbal).
Advanced English and Spanish proficiency (verbal and written).
Ability to thrive in a fast-changing environment and collaborate effectively with multidisciplinary teams.
University degree in Engineering, Medicine, Pharmacy, Biotechnology, Law, or another relevant scientific discipline.

Solicitud rápida

Refina tu búsqueda

clinical research empleos en tres cantos, md

Regulatory & Quality Lead – AI IVD Diagnostics

Delegado Derma y Estética - Madrid

Associate Medical Director- Neurology

Associate Pharmacovigilance Project Manager (Europe)

Senior Director, Drug Development

Senior Medical Information Associate Italian Language

CRA I-II in Madrid. Sponsor dedicated.

Senior Site Contract Associate - IQVIA Biotech

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

Senior Statistician

Senior Director / Executive Director Medical Writing

Medical Information Associate- Italian language

Artificial Intelligence Research Scientist

Access Field Head

Compliance - Senior Consultant (Life Science exp mandatory)

Medical Safety Director, Clinical Scientist

Sr Medical Project Manager

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

Core Information Offering Specialist - MedTech

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

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

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