20 publicaciones de empleo destacadas de clinical research en san sebastián de los reyes, md (¡Están contratando!)

Senior Director / Executive Director Medical Writing
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Liderazgo
Solicitud rápida
Artificial Intelligence Research Scientist
SpotLab —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Informática
Solicitud rápida
Product Data Officer - Medical Devicer (Fixed-Term Contract)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
7d
Core Information Offering Specialist - MedTech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Inglés
- Teletrabajo opcional
1d
Access Field Head
Novartis —Madrid, Madrid provincia
- De 109.800 € a 204.000 € al año
- Jornada completa
- Negociación
8d
Account Manager
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Ventas
- Servicio al cliente
- Grado
- Teletrabajo opcional
Senior Medical Information Associate Italian Language
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Servicio al cliente
- Inglés
- Habilidades de comunicación
Solicitud rápida
Senior Pharmacovigilance Officer, Team Lead/ Case Processing Manager- Medical Device experience needed
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Inglés
- Microsoft Office
- Gestión del tiempo
Solicitud rápida
Delegad@ Hospitalario - Madrid
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Habilidades organizativas
- Habilidades de comunicación
- Formación continua
Global Study Manager - Single Sponsor dedicated (in EMEA)
IQVIA —Madrid, Madrid provincia
- De 171.500 € a 404.600 € al año
- Jornada completa
- Inglés
- Investigación
- Máster
- Teletrabajo opcional
Risk Manager
Sinclair —San Fernando de Henares, Madrid provincia
- Trabajo híbrido
- Inglés
- Máster
Consultant – Global Advisory Services
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Máster
- Project management
Associate Pharmacovigilance Project Director (Delivery)- Europe
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Project management
- Gestión de conflictos
- Liderazgo
Solicitud rápida
3d
Delegad@ EREP-Madrid
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
Talent Acquisition Specialist EMEA
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Español
- Servicio al cliente
- Inglés
6d
Principal Statistician (Pharmacokinetics)
PSI CRO —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
Solicitud rápida
Medical Information Associate- Italian language
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Microsoft Word
- Microsoft Excel
- Servicio al cliente
Solicitud rápida
2d
Market Access Director Oncology
Regeneron —Madrid, Madrid provincia
- De 96.000 € a 160.000 € al año
- Trabajo híbrido
- Grado
- Seguro dental
- Vacaciones pagadas
Manager, Commercial Quality
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Microsoft Powerpoint
- Microsoft Word
- Enfermería
Solicitud rápida
7d
Senior Editor - The Lancet’s eBioMedicine
RELX —Madrid, Madrid provincia
- De 36.400 € a 63.600 € al año
- Jornada completa
- Doctorado
- Inglés
- Investigación

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Senior Director / Executive Director Medical Writing

PrimeVigilance -
Madrid, Madrid provincia

Solicitud rápida

Detalles del empleo

Jornada completa

Cualificaciones

Gestión de compliance
Liderazgo

Descripción completa del empleo

Company Description

Medicine moves forward here. So will you.

At PrimeVigilance, patient safety is not one part of the job. It is why we exist.

We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of every decision, from early development through to post-marketing surveillance. Increasingly, the value we create is not only in processing safety data but in interpreting it: spotting the signal that matters early and turning it into insight our clients can act on.

That work takes curious minds, problem-solvers and experts who care about getting it right. It also takes a culture worth staying for. Across Europe, North America, South America, Asia and Australia, we work in an environment built on kindness, flexibility, growth and belonging, where colleagues support one another and good ideas are heard wherever they come from.

If you want a role with real purpose, global reach and the chance to keep growing while you help protect patients, you will feel at home here. We would love to hear from you.

Job Description

The Senior Director / Executive Director Medical Writing is a senior management position, member of the Senior Leadership Team; Acts as Head of PV Medical Writing Group and has primary responsibility to ensure the contracted PV activities are appropriately performed in line with company policies/procedures and in compliance with global regulations.

Responsibilities

Lead the PV Medical Writing function, ensuring high-quality, compliant, and timely deliverables.
Manage and develop the PV Medical Writing team, fostering performance, engagement, and professional growth.
Drive quality, compliance, inspection readiness, and continuous improvement initiatives, including oversight of SOPs, KPIs, audits, and regulatory inspections.
Provide strategic PV medical writing expertise and subject matter leadership to clients, internal stakeholders, and project teams.
Support business development activities, including proposals, bid defenses, and client engagements.
Oversee departmental resources, budgets, and operational performance to ensure efficient service delivery.
Review regulatory safety responses and contribute to Risk Management Plans, aggregate reports, and other key pharmacovigilance deliverables.
Build and maintain strong client relationships, ensuring exceptional service and trusted partnerships.
Represent the organization externally through industry engagement, publications, presentations, and professional development activities.

Qualifications

The preferred candidate will have:

Extensive pharmacovigilance and PV Medical Writing experience, including leadership and people management of high-performing teams.
Deep knowledge of global pharmacovigilance regulations, with expertise in authoring and reviewing aggregate safety reports and PV procedures.
Proven experience supporting regulatory compliance, inspections, and pharmacovigilance system oversight, including QPPV or Deputy QPPV responsibilities.
Strong business acumen with experience supporting proposals, client engagements, and bid defense activities.
Excellent scientific, regulatory, and analytical capabilities, including translating complex clinical and safety data into clear, high-quality regulatory and scientific documents

Additional Information

When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.

We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here.

Quality: we hold ourselves to the standard patients deserve.
Integrity and trust: we do the right thing, especially when it is hard.
Drive and passion: we care about the outcome, because someone is waiting on it.
Agility and responsiveness: we move quickly, because patients cannot wait.
Belonging: everyone is welcome, and every voice counts.
Collaborative partnerships: we go further by going together.

We look forward to welcoming your application.

Solicitud rápida

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clinical research empleos en san sebastián de los reyes, md

Senior Director / Executive Director Medical Writing

Artificial Intelligence Research Scientist

Product Data Officer - Medical Devicer (Fixed-Term Contract)

Core Information Offering Specialist - MedTech

Access Field Head

Account Manager

Senior Medical Information Associate Italian Language

Senior Pharmacovigilance Officer, Team Lead/ Case Processing Manager- Medical Device experience needed

Delegad@ Hospitalario - Madrid

Global Study Manager - Single Sponsor dedicated (in EMEA)

Risk Manager

Consultant – Global Advisory Services

Associate Pharmacovigilance Project Director (Delivery)- Europe

Delegad@ EREP-Madrid

Talent Acquisition Specialist EMEA

Principal Statistician (Pharmacokinetics)

Medical Information Associate- Italian language

Market Access Director Oncology

Manager, Commercial Quality

Senior Editor - The Lancet’s eBioMedicine

Quiero recibir la alerta de empleo más reciente de clinical research en san sebastián de los reyes, md

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