20 publicaciones de empleo destacadas de clinical research en comunidad de madrid (¡Están contratando!)

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
Senior Site Contract Associate - IQVIA Biotech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Microsoft Office
- Grado
- Teletrabajo opcional
Study Start Up Associate II
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Seguro dental
- Seguro oftalmológico
12d
Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
Sr Medical Project Manager
Gilead Sciences —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Inglés
9d
Senior Director / Executive Director Medical Writing
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Liderazgo
Solicitud rápida
Delegad@ EREP-Madrid
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
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
Compliance - Senior Consultant (Life Science exp mandatory)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Máster
- Grado
Senior Statistician
PSI CRO —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Máster
Solicitud rápida
8d
Innovation manager Hematología
SpotLab —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Inglés
Solicitud rápida
Site Engagement Manager
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Grado
- Seguro dental
- Seguro oftalmológico
Central Monitoring Manager
PSI CRO —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Español
- Microsoft Excel
- Inglés
Solicitud rápida
Talent Acquisition Specialist EMEA
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Español
- Servicio al cliente
- Inglés
7d
Account Manager
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Ventas
- Servicio al cliente
- Grado
- Teletrabajo opcional
Consultant – Global Advisory Services
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Máster
- Project management
Business Development - AI for Hematology and Digital Pathology
SpotLab —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Español
- Hospital
- Inglés
Solicitud rápida
Team Lead, eCOA project management
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Project management
- Seguro dental
- Seguro oftalmológico
3d
Product Data Officer - Medical Devicer (Fixed-Term Contract)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
8d
Project Manager
Persei vivarium —Madrid, Madrid provincia
- PMP
- Project management
- Habilidades organizativas
Solicitud rápida

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

PrimeVigilance -
Madrid, Madrid provincia

Solicitud rápida

Detalles del empleo

Jornada completa

Cualificaciones

Inglés
Microsoft Office
Gestión del tiempo

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

Leads the team responsible for ICSR management for a selected project or group of projects as Team Leader and Line Manages ICSR staff
Ensures adequate distribution of tasks for assigned projects and teams and oversees the workflow process
Assures and exerts of activities leading to effective cooperation with clients in the area of ICSR Management
Contributes to achieving company´s goals and objectives
Works under supervision of ICSR Operational Lead
Role and Responsibilities
Providing support to other activities undertaken by the project team on behalf of the client and the company
Creates and maintains project specific KPIs for contracted ICSR activities (this includes optimizing procedures, trainings and any other actions to increase ICSR team efficiency)
Proposes process changes to ICSR Operational Lead
Manages ICSR deviations with ICSR Operational Lead support
Reviews trackers and timesheet data and ensures accuracy
Is involved in ICSR processing and 2nd QC of cases
Support other departments, as approved and instructed by ICSR Operational Lead
Operates as the assigned team SME
Supporting the RA & PV Network Department as needed, including acting as the LCPPV (Local Contact Person for Pharmacovigilance) for the specified country and taking on the role of PRLS (Person Responsible for Local Screening) for the designated language, as agreed with the line manager

Qualifications

Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance
Strong previous work experience in pharmacovigilance within which minimum 1 year of work experience in line manager role.
Medical Device experience required
Excellent communication (written and verbal) skills
Organization skills, including attention to details and multitasking
Delegation skills
Planning and time management
Technical skills
Team working
English – fluent (spoken, written)
Advanced literacy (MS Office)

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.

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

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Delegad@ EREP-Madrid

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Senior Statistician

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Central Monitoring Manager

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Account Manager

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Business Development - AI for Hematology and Digital Pathology

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

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Quiero recibir la alerta de empleo más reciente de clinical research en comunidad de madrid

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