20 publicaciones de empleo destacadas de de farmacia en sabadell, ct (¡Están contratando!)

Associate Clinical Trials Regulatory Manager, EMEA
IQVIA —Barcelona, Barcelona provincia
- Investigación
- Desarrollo de negocios
- Project management
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- Jornada completa
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- Habilidades organizativas
Head of Medical Rare Diseases
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- Español
- Doctorado
- Inglés
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Instituto Grifols SA —Sant Cugat del Vallès, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Microsoft Excel
- Inglés
- Máster
1d
Training Specialist
Instituto Grifols SA —Parets del Vallès, Barcelona provincia
- Jornada completa
- Microsoft Office
- Grado
- Habilidades organizativas
- Formación continua
- Flexibilidad horaria
Quality Assurance Laboratory Manager
Grifols SA —Sant Cugat del Vallès, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Grado
Rare Disease & Oncology Medical Affairs Manager
AstraZeneca —Barcelona, Barcelona provincia
- Doctorado
- Máster
- Grado
6d
Medical Director, Global Patient Safety
Alexion Pharmaceuticals,Inc. —Barcelona, Barcelona provincia
- Microsoft Powerpoint
- Microsoft Word
- Enfermería
Immunology Alliance Franchise Medical Head Iberia
Sanofi —Barcelona, Barcelona provincia
- Español
- Doctorado
- Máster
Coordinador/a Tècnics de Farmàcia
Hospital General de Granollers —Granollers, Barcelona provincia
- Hospital
- Microsoft Office
- Habilidades de comunicación
Solicitud rápida
Technical Auxiliary CAPS Trainee Rubí
B. Braun SE —Rubí, Barcelona provincia
- Jornada completa
- Grado
- Habilidades organizativas
- Contrato en prácticas
- Parking gratuito
- Oportunidades de crecimiento y desarrollo profesional
8d
Pharmacokinetic Scientist
Kymos Group —Barcelona, Barcelona provincia
- Español
- Doctorado
- Inglés
9d
Associate Director, Centralized Content
Alexion Pharmaceuticals,Inc. —Barcelona, Barcelona provincia
- Microsoft Excel
- Doctorado
- Oficina
8d
QA SENIOR MANAGER / QP DEPUTY ALMIRALL
Almirall —Sant Andreu de la Barca, Barcelona provincia
- Jornada completa
- Inglés
- Grado
- Control de calidad
- Oportunidades de crecimiento y desarrollo profesional
2d
Commercial & Academic Clinical Research Director
VHIR —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Español
- Doctorado
- Hospital
Técnico de PPWR - 40h - Barcelona
Miin Cosmetics —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Máster
- Grado
Solicitud rápida
9d
ANALISTA DE CONTROL DE CALIDAD
Alivira —Caldes de Montbui, Barcelona provincia
- Jornada completa
- Control de calidad
Solicitud rápida
Associate Director, Patient Safety Scientist
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Enfermería
- Microsoft Excel
- Doctorado
9d
Técnico/a Sintesis Química I+D
Moehs Ibérica —Barcelona, Barcelona provincia
- Doctorado
- Grado
- Oportunidades de crecimiento y desarrollo profesional
GLOBAL MEDICAL OPERATIONS MANAGER
Almirall —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Máster
- Grado

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Associate Clinical Trials Regulatory Manager, EMEA

IQVIA -
Barcelona, Barcelona provincia

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Detalles del empleo

Hace 2 días

Cualificaciones

Investigación clínica
Investigación
Desarrollo de negocios
Project management
Grado
Farmacia

Descripción completa del empleo

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.

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de farmacia empleos en sabadell, ct

Associate Clinical Trials Regulatory Manager, EMEA

Quality Assurance Trainee

Head of Medical Rare Diseases

TECHNICAL DRUG SAFETY OFFICER

Training Specialist

Quality Assurance Laboratory Manager

Rare Disease & Oncology Medical Affairs Manager

Medical Director, Global Patient Safety

Immunology Alliance Franchise Medical Head Iberia

Coordinador/a Tècnics de Farmàcia

Technical Auxiliary CAPS Trainee Rubí

Pharmacokinetic Scientist

Associate Director, Centralized Content

QA SENIOR MANAGER / QP DEPUTY ALMIRALL

Commercial & Academic Clinical Research Director

Técnico de PPWR - 40h - Barcelona

ANALISTA DE CONTROL DE CALIDAD

Associate Director, Patient Safety Scientist

Técnico/a Sintesis Química I+D

GLOBAL MEDICAL OPERATIONS MANAGER

Quiero recibir la alerta de empleo más reciente de de farmacia en sabadell, ct

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