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
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
Business Development Manager – Medical Affairs Solutions (IQVIA Pharma Review)
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Desarrollo de negocios
Analyst, PAE
Alira Health —Barcelona, Barcelona provincia
- De 20.000 € a 22.000 € al año
- Jornada completa
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Sponsor Dedicated Sr. SSU CTA - Hybrid Barcelona
Syneos - Clinical and Corporate - Prod —Barcelona, Barcelona provincia
- Jornada completa
- Investigación
3d
Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
Core Information Offering Specialist - MedTech
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Inglés
- Teletrabajo opcional
1d
Principal, Health Economics, Health Technology Assessment
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Microsoft Excel
- Máster
- Inteligencia artificial
Precision Medicine Director
Novartis —Barcelona, Barcelona provincia
- De 85.100 € a 158.100 € al año
- Jornada completa
- Trabajo híbrido
- Investigación
- Liderazgo
- Plan de pensiones
Study Start Up Associate II
ICON Plc —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Seguro dental
- Seguro oftalmológico
10d
Project Manager
Barcelona Institute for Global Health (ISGlobal) —Barcelona, Barcelona provincia
- Media jornada
- Español
- Doctorado
- Inglés
9d
Sponsor Dedicated Sr. SSU CTA - Hybrid Barcelona
サイネオス・ヘルス —Barcelona, Barcelona provincia
- Investigación
2d
Senior Director, Drug Development
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Investigación
- Teletrabajo opcional
Associate Consultant
Alira Health —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Data Steward (Barcelona)
EBMT —Barcelona, Barcelona provincia
- De 31.574 € a 34.595 € al año
- Jornada completa
- Trabajo híbrido
- Inglés
- Investigación
- SQL
20h
SSU CRA II Barcelona. Sponsor dedicated
サイネオス・ヘルス —Barcelona, Barcelona provincia
- Grado
7d
Medical Director - Ophthalmology
Fortrea —Barcelona, Barcelona provincia
- Turno de 8 horas
- Teletrabajo
- Investigación
Trial Vendor Associate Director
Novartis —Barcelona, Barcelona provincia
- De 63.600 € a 118.000 € al año
- Jornada completa
7d
Data Science Consultant, Discovery & Translational Science
Clarivate —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Doctorado
- Inglés

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Clinical QA Manager

ICON Plc -
Barcelona, Barcelona provincia

Solicitar ahora

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

Associate Manager – Global Pricing (HTA and Pricing Reporting)

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Analyst, PAE

Sponsor Dedicated Sr. SSU CTA - Hybrid Barcelona

Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience

Core Information Offering Specialist - MedTech

Principal, Health Economics, Health Technology Assessment

Precision Medicine Director

Study Start Up Associate II

Project Manager

Sponsor Dedicated Sr. SSU CTA - Hybrid Barcelona

Senior Director, Drug Development

Associate Consultant

Data Steward (Barcelona)

SSU CRA II Barcelona. Sponsor dedicated

Medical Director - Ophthalmology

Trial Vendor Associate Director

Data Science Consultant, Discovery & Translational Science

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

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