20 publicaciones de empleo destacadas de key people pharmaceutical en barcelona, ct (¡Están contratando!)

Associate Clinical Trials Regulatory Manager, EMEA
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Investigación
- Desarrollo de negocios
- Project management
- Teletrabajo opcional
Associate Director, MA Portfolio & Programme Management
Novartis —Barcelona, Barcelona provincia
- De 73.100 € a 135.700 € al año
- Jornada completa
- Doctorado
- Liderazgo
- Negociación
7d
Senior Director, Drug Development
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Investigación
- Teletrabajo opcional
Global Trial Delivery Lead - Sponsor Dedicated
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Investigación
- Máster
- Teletrabajo opcional
Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Doctorado
- Investigación
- Máster
District Manager - Cardiovascular, Barcelona - Valencia
Amgen —Barcelona, Barcelona provincia
- De 101.509,55 € a 137.336,45 € al año
- Doctorado
- Ventas
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Associate Director, Data & Analytics – Delivery Region Europe
Novartis —Barcelona, Barcelona provincia
- De 52.400 € a 97.400 € al año
- Jornada completa
- SQL
- Scripting
- Python
12d
Manager Risk Management
Novartis —Barcelona, Barcelona provincia
- De 46.300 € a 86.100 € al año
- Jornada completa
- Doctorado
- Inglés
- Máster
1d
Lead Data Scientist - BCN/MAD/Munich
ailylabs —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Oficina
- SQL
- Machine learning
Solicitud rápida
QA Batch Release Trainee
Kymos Group —Cerdanyola del Vallès, Barcelona provincia
- Microsoft Word
- Microsoft Excel
- Inglés
Digital ERP Program Lead
Opella Healthcare Group —Barcelona, Barcelona provincia
- Jornada completa
- Informática
- Sistemas ERP
- Máster
Competition Compliance Manager
Grifols SA —Sant Cugat del Vallès, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Español
- Inglés
Immunology TA Access Strategy Manager
Novartis —Barcelona, Barcelona provincia
- De 59.600 € a 110.800 € al año
- Jornada completa
- Español
- Inglés
- Project management
2d
Director, Regulatory Affairs Strategy - Cell Therapy
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Oficina
- Habilidades de presentación
Apprentice Business Continuity, Risk Management
dsm-firmenich —Barcelona, Barcelona provincia
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Associate Manager – Global Pricing (HTA and Pricing Reporting)
Sanofi —Barcelona, Barcelona provincia
- De 48.000 € a 64.000 € al año
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Inglés
Quality Manager
URIACH —Sant Cugat del Vallès, Barcelona provincia
- Español
- Microsoft Excel
- Inglés
Solicitud rápida
Senior Business Analyst
Novartis —Barcelona, Barcelona provincia
- De 41.900 € a 77.700 € al año
- Jornada completa
- Informática
- Inglés
- Habilidades de análisis
2d
CISOC Application Security Engineer (Pharmaceutical Sector)
Omega CRM —Sant Cugat del Vallès, Barcelona provincia
- Trabajo híbrido
- Salesforce
- DevOps
- Inglés
Solicitud rápida
6d
Director, AQS Strategic Project Management Lead
Novartis —Barcelona, Barcelona provincia
- De 85.100 € a 158.100 € al año
- Jornada completa
- Investigación
- Project management
7d

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Associate Clinical Trials Regulatory Manager, EMEA

IQVIA -
Barcelona, Barcelona provincia

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Detalles del empleo

Jornada completa

Beneficios

Teletrabajo opcional

Cualificaciones

Investigación clínica
Investigación
Desarrollo de negocios
Project management
Grado
Farmacia

Descripción completa del empleo

Barcelona, 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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key people pharmaceutical empleos en barcelona, ct

Associate Clinical Trials Regulatory Manager, EMEA

Associate Director, MA Portfolio & Programme Management

Senior Director, Drug Development

Global Trial Delivery Lead - Sponsor Dedicated

Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting

District Manager - Cardiovascular, Barcelona - Valencia

Associate Director, Data & Analytics – Delivery Region Europe

Manager Risk Management

Lead Data Scientist - BCN/MAD/Munich

QA Batch Release Trainee

Digital ERP Program Lead

Competition Compliance Manager

Immunology TA Access Strategy Manager

Director, Regulatory Affairs Strategy - Cell Therapy

Apprentice Business Continuity, Risk Management

Associate Manager – Global Pricing (HTA and Pricing Reporting)

Quality Manager

Senior Business Analyst

CISOC Application Security Engineer (Pharmaceutical Sector)

Director, AQS Strategic Project Management Lead

Quiero recibir la alerta de empleo más reciente de key people pharmaceutical en barcelona, ct

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