Clinical Research Associate Ii

Icon Clinical Plc; Barcelona; Presencial; EUR 34.000 - 58.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes and wel

Learning and development opportunities

Descripción de la vacante

ICON Clinical PLC, con sede en Barcelona, busca un Clinical Research Associate II para unirse a nuestro equipo dinámico en España. El rol implica diseñar y analizar ensayos clínicos, interpretar datos médicos y contribuir al avance de tratamientos innovadores.

El candidato ideal posee al menos 2 años de experiencia como CRA, conocimiento de ICH-GCP, excelentes habilidades organizativas y de comunicación, capacidad para viajar aproximadamente el 60% y trabajar tanto de forma independiente como en

Formación

• Título universitario en campo científico o sanitario.
• Al menos 2 años de experiencia como Clinical Research Associate.
• Conocimiento de procesos de ensayos clínicos y guías ICH-GCP.
• Excelentes habilidades organizativas y de comunicación.
• Disponibilidad para viajar ≈60% (nacional e internacional).
• Buen nivel de inglés.

Responsabilidades

• Realizar visitas de calificación, iniciación, monitorización y cierre de ensayos clínicos.
• Velar por el cumplimiento del protocolo, integridad de datos y seguridad de los pacientes.
• Colaborar con investigadores y personal de los sitios para apoyar la conducción del estudio.
• Revisar datos y resolver consultas para mantener datos de alta calidad.
• Contribuir a la preparación y revisión de documentación del estudio (protocolos, informes clínicos).

Conocimientos

Organisational skills

Communication skills

Travel willingness

Independent & collaborative work

ICH-GCP knowledge

Attention to detail

Educación

Bachelor's degree in a scientific or healthcare-related field

Descripción del empleo

Clinical Research Associate II Icon Clinical PLC Barcelona, Província de Barcelona, Spain

Descripción del trabajo

CRA IIICON 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.

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team.

As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

• 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

• 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 organisational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license.
• Good level of English.
• 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 here.

Summary

Location: Spain, Madrid; Spain, Barcelona

Type: Full time