20 publicaciones de empleo destacadas de clinical trial en barcelona, ct (¡Están contratando!)

Clinical Research Associate
ICON Plc —Barcelona, Barcelona provincia
- Jornada completa
- Investigación
- Grado
- Seguro dental
- Seguro oftalmológico
Clinical Trial Manager II. Barcelona or Madrid. FSP
Syneos - Clinical and Corporate - Prod —Barcelona, Barcelona provincia
- Jornada completa
- Grado
- Gestión de conflictos
14d
Senior Clinical Research Associate
Alira Health —Barcelona, Barcelona provincia
- De 55.000 € a 65.000 € al año
- Jornada completa
- Servicio al cliente
- Inglés
- Investigación
plaça de Clinical Trial Assistant (CTA) CIDO
Fundació Institut d'Investigació i Innovació Parc Taulí (I3PT) —Comarca del Vallès Occidental, Barcelona provincia
13d
Associate Clinical Programmer - Clinical Data Operations
Novartis —Barcelona, Barcelona provincia
- De 27.900 € a 51.900 € al año
- Jornada completa
- Informática
- Inglés
- Investigación
5d
Clinical Research Associate 2 - CFSP
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Microsoft Office
- Teletrabajo opcional
Clinical Pricing & Payments Senior Associate _ Pricing
ICON Plc —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Investigación
- Grado
- Seguro dental
- Seguro oftalmológico
6d
Associate Clinical Programmer - Clinical Study Data, Risk based Quality Management & Monitoring
Novartis —Barcelona, Barcelona provincia
- De 27.900 € a 51.900 € al año
- Jornada completa
- Informática
- SQL
- Grado
8d
Clinical Research Associate 2 - Multi-Sponsor - Based in Barcelona
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Microsoft Office
- Teletrabajo opcional
Medical Science Liaison - Vaccines
CSL Seqirus —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Doctorado
- Inglés
Clinical Trial Safety Scientist (FSP - Permanent Home Based)
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Doctorado
- Gestión del tiempo
- Teletrabajo opcional
Clinical Biospecimen Scientist - Single Sponsor Dedicated
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Grado
- Teletrabajo opcional
Expert Clinical Programmer - Clinical Study Data, Risk based Quality Management & Monitoring
Novartis —Barcelona, Barcelona provincia
- De 36.100 € a 67.100 € al año
- Jornada completa
- Informática
- SQL
- Project management
8d
Junior Project Coordinator in the Central Lab department
Anapharm Bioanalytics —Barcelona, Barcelona provincia
- Microsoft Word
- Microsoft Excel
- Inglés
Clinical Document Migrations Manager
Novartis —Barcelona, Barcelona provincia
- De 46.300 € a 86.100 € al año
- Jornada completa
- Agile
Clinical Research Monitor (Rheumatology Research Group)
VHIR —Barcelona, Barcelona provincia
- De 24.000 € a 27.000 € al año
- Jornada completa
- Microsoft Word
- Hospital
- Procesamiento de textos
12d
Clinical Trial Excellence Project Manager
Novartis —Barcelona, Barcelona provincia
- Jornada completa
- Investigación
- Grado
6d
Study Support Assistant
ICON Plc —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Seguro dental
- Seguro oftalmológico
1d
Collaborative research and clinical operations Project Manager
Hospital Sant Joan de Déu Barcelona —Esplugues de Llobregat, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Máster
Associate Director - Clinical Data Analytics & Technology
Novartis —Barcelona, Barcelona provincia
- De 63.600 € a 118.000 € al año
- Jornada completa
- Inglés
- Investigación
- Oficina
8d

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Clinical Research Associate

ICON Plc -
Barcelona, Barcelona provincia

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Detalles del empleo

Jornada completa

Beneficios

Seguro dental
Seguro oftalmológico
Plan de pensiones

Cualificaciones

Investigación clínica
Investigación
Grado

Descripción completa del empleo

Clinical Research Associate II

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 CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Collaborating with investigators and site staff to facilitate smooth study conduct.
Performing data review and resolution of queries to maintain high-quality clinical data.
Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your Profile:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required qualifications and experience:

Bachelor's degree in a scientific or healthcare-related field.
Minimum of 2 years of experience as a Clinical Research Associate.
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
Strong organizational and communication skills, with attention to detail.
Ability to work independently and collaboratively in a fast-paced environment.
Willingness to travel as required (approximately 60%)

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 trial empleos en barcelona, ct

Clinical Research Associate

Clinical Trial Manager II. Barcelona or Madrid. FSP

Senior Clinical Research Associate

plaça de Clinical Trial Assistant (CTA) CIDO

Associate Clinical Programmer - Clinical Data Operations

Clinical Research Associate 2 - CFSP

Clinical Pricing & Payments Senior Associate _ Pricing

Associate Clinical Programmer - Clinical Study Data, Risk based Quality Management & Monitoring

Clinical Research Associate 2 - Multi-Sponsor - Based in Barcelona

Medical Science Liaison - Vaccines

Clinical Trial Safety Scientist (FSP - Permanent Home Based)

Clinical Biospecimen Scientist - Single Sponsor Dedicated

Expert Clinical Programmer - Clinical Study Data, Risk based Quality Management & Monitoring

Junior Project Coordinator in the Central Lab department

Clinical Document Migrations Manager

Clinical Research Monitor (Rheumatology Research Group)

Clinical Trial Excellence Project Manager

Study Support Assistant

Collaborative research and clinical operations Project Manager

Associate Director - Clinical Data Analytics & Technology

Quiero recibir la alerta de empleo más reciente de clinical trial en barcelona, ct

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