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

Associate Clinical Trials Regulatory Manager, EMEA
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- Investigación
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Associate Director, Centralized Content
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- Microsoft Excel
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Commercial & Academic Clinical Research Director
VHIR —Barcelona, Barcelona provincia
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Almirall —Sant Andreu de la Barca, Barcelona provincia
- Jornada completa
- Inglés
- Grado
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Associate Director, Patient Safety Scientist
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Enfermería
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GLOBAL MEDICAL OPERATIONS MANAGER
Almirall —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Máster
- Grado
Biopharmaceutical Analysis Manager
Kymos Group —Barcelona, Barcelona provincia
- Doctorado
- Inglés
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Técnico de PPWR - 40h - Barcelona
Miin Cosmetics —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Máster
- Grado
Solicitud rápida
8d
Validation Technician
Grifols SA —Parets del Vallès, Barcelona provincia
- Jornada completa
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Medical Writer Supervisor
Remedy Edge Spain —Barcelona, Barcelona provincia
- Español
- Doctorado
- Inglés
Solicitud rápida
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Farmacéutico/a Sustituto/a
Farmacia Ruth Calvo Sanchez —La Llagosta, Barcelona provincia
- Grado
Solicitud rápida
9d
Quality Assurance Trainee
Ferrer —Sant Cugat del Vallès, Barcelona provincia
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- Trabajo híbrido
- Inglés
- Microsoft Office
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MEDICAL AFFAIRS SENIOR MANAGER
Almirall —Barcelona, Barcelona provincia
- Jornada completa
- Doctorado
- Inglés
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Complaints Specialist
Diagnóstic Grifols SA —Parets del Vallès, Barcelona provincia
- Jornada completa
- Teletrabajo
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plaça de Tècnic en laboratori CIDO
Fundació Bosch Gimpera —Barcelona, Barcelona provincia
- Español
- Inglés
1h

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

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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

Training Specialist

Rare Disease & Oncology Medical Affairs Manager

Medical Director, Global Patient Safety

Immunology Alliance Franchise Medical Head Iberia

Pharmacokinetic Scientist

Associate Director, Centralized Content

Commercial & Academic Clinical Research Director

QA SENIOR MANAGER / QP DEPUTY ALMIRALL

Associate Director, Patient Safety Scientist

GLOBAL MEDICAL OPERATIONS MANAGER

Biopharmaceutical Analysis Manager

Técnico de PPWR - 40h - Barcelona

Validation Technician

Medical Writer Supervisor

Farmacéutico/a Sustituto/a

Quality Assurance Trainee

MEDICAL AFFAIRS SENIOR MANAGER

Complaints Specialist

plaça de Tècnic en laboratori CIDO

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

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