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

Associate Clinical Trials Regulatory Manager, EMEA
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Desarrollo de negocios
- Project management
- Teletrabajo opcional
Clinical Biospecimen Scientist - Single Sponsor Dedicated
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Grado
- Teletrabajo opcional
Associate Safety Project Manager
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Ventas
- Investigación
- Project management
- Teletrabajo opcional
7d
Senior Field Clinical Research Engineer
Boston Scientific —Madrid, Madrid provincia
- Máster
- Grado
2d
Regional Sales Manager, Southern Europe
ConcertAI —Madrid, Madrid provincia
- Teletrabajo
- Español
- Ventas
- Inglés
Manager, AI Sales & Customer-Facing Capability Upskilling
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Ventas
- Project management
- Grado
- Teletrabajo opcional
Senior Generative AI Engineer
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Azure
- Informática
- Máster
13d
Clinical Project Manager / Senior Clinical Project Manager
Precision for Medicine —Madrid, Madrid provincia
- Teletrabajo
- Microsoft Powerpoint
- Inglés
- Investigación
Solicitud rápida
Clinical Project Manager / Senior Clinical Project Manager
Precision Medicine Group —Madrid, Madrid provincia
- Teletrabajo
- Microsoft Powerpoint
- Inglés
- Investigación
Clinical Research Associate
Opis s.r.l. —Madrid, Madrid provincia
- Hasta 48.000 € al año
- Jornada completa
- Inglés
- Microsoft Office
9d
Nutriasesor Hospital y Residencias - Madrid
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Hospital
- Habilidades de comunicación
- Formación continua
- Ayuda al desarrollo profesional
23h
Nutriasesor@ - Madrid
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Máster
- Grado
- Habilidades organizativas
- Formación continua
- Ayuda al desarrollo profesional
23h
Research Nurse - Madrid
IQVIA —Madrid, Madrid provincia
- Media jornada
- Microsoft Word
- Microsoft Excel
- Microsoft Access
9d
PV Officer (experience in Medical devices required)
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Inglés
- Gestión del tiempo
Solicitud rápida
11d
Sr Director, Drug Development Lead
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Doctorado
- Teletrabajo opcional
3d
Safety Associate Medical Information Coordinator with Greek and French, German or Italian
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Microsoft Office
- Grado
- Teletrabajo opcional
7d
Principal, Regulatory Science and Strategy - Real World Solutions
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Inglés
- Máster
- Teletrabajo opcional
23h
Lead Consultant - Evidence Synthesis
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Máster
- Liderazgo
- Seguro dental
- Seguro oftalmológico
7d
HR Coordinator
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Español
- Microsoft Office
- Grado
10d
Product Data Officer (Medical Devices) - Hybrid / Temporary Contract
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
8d

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

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Associate Clinical Trials Regulatory Manager, EMEA

IQVIA -
Madrid, Madrid provincia

Solicitar ahora

Detalles del empleo

Jornada completa

Beneficios

Teletrabajo opcional

Cualificaciones

Investigación clínica
Investigación
Desarrollo de negocios
Project management
Grado
Farmacia

Descripción completa del empleo

Madrid, Spain | Full time | Home-based | R1556227

Associate Clinical Trials Regulatory Manager

EMEA

Homebased

Job Summary

The Associate Clinical Trials Regulatory Manager provides regulatory support and oversight for clinical trial submissions across global programs. This role is responsible for preparing and reviewing regulatory documentation, managing submissions, ensuring regulatory compliance, and supporting clients and internal stakeholders throughout the clinical trial lifecycle. This is not a people manager role, but a process management position.

Key Responsibilities

Serve as the Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects and programs.
Provide regulatory oversight and strategic guidance to internal and external stakeholders.
Review scientific and regulatory documentation, conduct gap analyses, and provide recommendations.
Author and/or review key regulatory documents, including Investigational Medicinal Product Dossiers (IMPDs) and clinical trial justifications.
Coordinate and support European centralized submissions and global country submissions.
Ensure project deliverables are completed on time, within scope, and in compliance with regulatory requirements.
Maintain accurate records in internal systems, databases, and tracking tools in accordance with SOPs.
Support business development activities by providing regulatory expertise.
Deliver regulatory training and presentations as required.
Mentor junior team members and contribute to departmental knowledge sharing initiatives.

Qualifications and Experience

Bachelor's degree in Life Sciences, Pharmacy, Regulatory Affairs, or a related field.
Typically 3–5 years of experience in Regulatory Affairs within the pharmaceutical, biotechnology, CRO, or clinical research industry.
Experience supporting clinical trial submissions and regulatory documentation.
Strong scientific writing, document review, project management, and stakeholder engagement skills.
Advanced knowledge of clinical trial regulations and regulatory submission processes.

Knowledge & Competencies

Advanced knowledge of regulatory affairs and clinical trial submission requirements.
Strong analytical and problem-solving skills.
Excellent communication and collaboration abilities.
Ability to work independently and manage multiple priorities in a fast-paced environment.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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clinical research empleos en la moraleja, md

Associate Clinical Trials Regulatory Manager, EMEA

Clinical Biospecimen Scientist - Single Sponsor Dedicated

Associate Safety Project Manager

Senior Field Clinical Research Engineer

Regional Sales Manager, Southern Europe

Manager, AI Sales & Customer-Facing Capability Upskilling

Senior Generative AI Engineer

Clinical Project Manager / Senior Clinical Project Manager

Clinical Project Manager / Senior Clinical Project Manager

Clinical Research Associate

Nutriasesor Hospital y Residencias - Madrid

Nutriasesor@ - Madrid

Research Nurse - Madrid

PV Officer (experience in Medical devices required)

Sr Director, Drug Development Lead

Safety Associate Medical Information Coordinator with Greek and French, German or Italian

Principal, Regulatory Science and Strategy - Real World Solutions

Lead Consultant - Evidence Synthesis

HR Coordinator

Product Data Officer (Medical Devices) - Hybrid / Temporary Contract

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

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