20 publicaciones de empleo destacadas de clinical research en castelldefels, ct (¡Están contratando!)

Clinical QA Manager
ICON Plc —Barcelona, Barcelona provincia
- Jornada completa
- Grado
- Seguro dental
- Seguro oftalmológico
Senior Medical Writer
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Doctorado
- Máster
- Grado
- Teletrabajo opcional
Laboratory Manager
VHIR —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Doctorado
- Hospital
Risk Surveillance Lead
Novartis —Barcelona, Barcelona provincia
- De 63.600 € a 118.000 € al año
- Jornada completa
- Inglés
- Oficina
- Grado
Epidemiologist (real world country operations)
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Associate Director, Global Health Economics & Outcomes Research
AstraZeneca —Barcelona, Barcelona provincia
- Doctorado
8d
Study Director Team Lead
Novartis —Barcelona, Barcelona provincia
- De 74.200 € a 137.800 € al año
- Jornada completa
- Investigación
- Project management
- Grado
9d
Associate Director - Clinical Data Analytics & Technology
Novartis —Barcelona, Barcelona provincia
- De 63.600 € a 118.000 € al año
- Jornada completa
- Inglés
- Investigación
- Oficina
Translation Project Manager – Linguistic Validation and eCOA
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Grado
- Teletrabajo opcional
Medical Safety Lead - CRM
Novartis —Barcelona, Barcelona provincia
- De 69.000 € a 128.100 € al año
- Jornada completa
- Enfermería
- Inglés
- Inteligencia artificial
1d
Sales Application Specialist Biotechnology
Werfen —Barcelona, Barcelona provincia
- Jornada completa
- Ventas
- Inglés
- Investigación
Amics del VHIR - Institutional call for the incorporation of Early-stage (R1) researchers
VHIR —Barcelona, Barcelona provincia
- De 19.563 € a 25.079 € al año
- Microsoft Excel
- Doctorado
- Hospital
7d
Study Start-Up Lead
ICON Plc —Barcelona, Barcelona provincia
- Jornada completa
- Investigación
- Liderazgo
- Seguro dental
- Seguro oftalmológico
16h
Global Program Safety Lead - CRM
Novartis —Barcelona, Barcelona provincia
- De 85.100 € a 158.100 € al año
- Jornada completa
- CRM software
- Doctorado
- Inglés
1d
Senior Staff - Medical & Scientific Affairs Liaison - Acute Care
Beckman Coulter Diagnostics —Barcelona, Barcelona provincia
- Jornada completa
- Doctorado
- Ventas
- Investigación
- Vacaciones pagadas
Postdoctoral Fellow (Ref. PD/26/11)
IRB Barcelona —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Doctorado
- Inglés
10d
Senior Statistician
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Doctorado
- Inglés
Lead Data Scientist - BCN/MAD/Munich
ailylabs —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Oficina
- SQL
- Machine learning
Solicitud rápida
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
Medical Optics Group: Post-doctoral position in applications of near-infrared spectroscopy and diffuse correlation spectroscopy in critical care
The Institute of Photonic Sciences (ICFO) —Castelldefels, Barcelona provincia
- Doctorado
- Hospital

Quiero recibir la alerta de empleo más reciente de clinical research en castelldefels, ct

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Clinical QA Manager

ICON Plc -
Barcelona, Barcelona provincia

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Detalles del empleo

Jornada completa

Beneficios

Seguro dental
Seguro oftalmológico
Plan de pensiones

Cualificaciones

Grado

Descripción completa del empleo

Clinical QA manager

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Clinical QA Manager at ICON, you will be is responsible for ensuring robust oversight of clinical trial compliance at the country and site level. This role applies a risk-based approach to proactively identify, evaluate,
and manage compliance risks, ensuring adherence to Good Clinical Practice (GCP), company procedures, and regulatory requirements. The role partners closely with country, regional and global stakeholders to safeguard
patient safety, data integrity, and inspection readiness.

What You Will Do:

Your focus will be on coordinating clinical quality assurance and compliance delivery, resolving issues, and developing team capability.

Key responsibilities include:

Developing and implementing quality assurance strategies and processes to support clinical trial activities.
Conducting quality assessments and audits to ensure compliance with regulatory standards and guidelines.
Collaborating with project teams to identify and address quality issues and implement corrective actions as needed.
Providing guidance and support to staff regarding quality assurance policies, procedures, and best practices.
Contributing to the development and maintenance of quality management systems and documentation.

Your Profile:

You will have solid quality assurance and compliance experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

Bachelor's degree in a relevant discipline
Minimum of 5 years of experience in quality assurance within the pharmaceutical, biotechnology, or CRO industry.
Knowledge of regulatory requirements and guidelines governing clinical trials (e.g., ICH-GCP, FDA regulations).
Strong analytical and problem-solving skills, with the ability to identify and resolve quality issues effectively.
Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and stakeholders.
Willingness to travel as required (approximately 35%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request .

Are you a current ICON Employee?

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clinical research empleos en castelldefels, ct

Clinical QA Manager

Senior Medical Writer

Laboratory Manager

Risk Surveillance Lead

Epidemiologist (real world country operations)

Associate Director, Global Health Economics & Outcomes Research

Study Director Team Lead

Associate Director - Clinical Data Analytics & Technology

Translation Project Manager – Linguistic Validation and eCOA

Medical Safety Lead - CRM

Sales Application Specialist Biotechnology

Amics del VHIR - Institutional call for the incorporation of Early-stage (R1) researchers

Study Start-Up Lead

Global Program Safety Lead - CRM

Senior Staff - Medical & Scientific Affairs Liaison - Acute Care

Postdoctoral Fellow (Ref. PD/26/11)

Senior Statistician

Lead Data Scientist - BCN/MAD/Munich

Associate Manager – Global Pricing (HTA and Pricing Reporting)

Medical Optics Group: Post-doctoral position in applications of near-infrared spectroscopy and diffuse correlation spectroscopy in critical care

Quiero recibir la alerta de empleo más reciente de clinical research en castelldefels, ct

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