20 publicaciones de empleo destacadas de clinical project en madrid, md (¡Están contratando!)

Associate Clinical Trials Regulatory Manager, EMEA
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Desarrollo de negocios
- Project management
- Teletrabajo opcional
National Sales Manager - Medical
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Microsoft Office
- Grado
Senior Feasibility Associate / Feasibility Manager
Precision for Medicine —Madrid, Madrid provincia
- Teletrabajo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Solicitud rápida
Associate Biostatistics Director - FSP (Permanent Home-based)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Investigación
- Máster
- Teletrabajo opcional
Director, Medical Safety
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Liderazgo
- Teletrabajo opcional
9d
Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
Director Business Development - Oncology
TFS HealthScience —Madrid, Madrid provincia
- Teletrabajo
- Español
- Ventas
- Inglés
Solicitud rápida
Innovation manager Hematología
SpotLab —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Inglés
Solicitud rápida
Medical Monitor (Gastroenterology)
PSI CRO —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Investigación
- Microsoft Office
Solicitud rápida
5d
Risk Manager
Sinclair —San Fernando de Henares, Madrid provincia
- Trabajo híbrido
- Inglés
- Máster
Senior Director, Commercial Sales & Operations, Brand Outsourcing & HCP Engagement
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Ventas
- Liderazgo
Senior Press Relations & Social Media Manager
Vantive —Madrid, Madrid provincia
- Español
- Inglés
- Grado
6d
Senior Director / Executive Director Medical Writing
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Liderazgo
Solicitud rápida
12d
Senior Feasibility Associate / Feasibility Manager
Precision Medicine Group —Madrid, Madrid provincia
- Teletrabajo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Global Team Leader - IVDR
SGS —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Inglés
- Investigación
- Oficina
Solicitud rápida
Software Development Engineer - Cronos
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Informática
- DevOps
- SQL
- Teletrabajo opcional
Software Engineer for Healthcare Sector Projects
GMV —Tres Cantos, Madrid provincia
- Trabajo híbrido
- Seguro dental
5d
Proposals Manager - Pharmacovigilance
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Inglés
- Investigación
Solicitud rápida
Principal Statistical Programmer - FSP (Permanent Homebased) m/w/d
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Informática
- Grado
- Teletrabajo opcional
Global Product Manager Implant Scanning
Straumann Group —La Moraleja, Madrid provincia
- Jornada completa
- Marketing
- Inglés
- Desarrollo de software

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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 project empleos en madrid, md

Associate Clinical Trials Regulatory Manager, EMEA

National Sales Manager - Medical

Senior Feasibility Associate / Feasibility Manager

Associate Biostatistics Director - FSP (Permanent Home-based)

Director, Medical Safety

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

Director Business Development - Oncology

Innovation manager Hematología

Medical Monitor (Gastroenterology)

Risk Manager

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

Senior Press Relations & Social Media Manager

Senior Director / Executive Director Medical Writing

Senior Feasibility Associate / Feasibility Manager

Global Team Leader - IVDR

Software Development Engineer - Cronos

Software Engineer for Healthcare Sector Projects

Proposals Manager - Pharmacovigilance

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

Global Product Manager Implant Scanning

Quiero recibir la alerta de empleo más reciente de clinical project en madrid, md

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