CRA II – Multi-Sponsor Clinical Trials (Spain)

IQVIA

Barcelona

Presencial

EUR 45.000 - 65.000

Jornada completa

Hace 2 días
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Descripción de la vacante

IQVIA Spain in Barcelona is seeking a Clinical Research Associate to join our Sponsor dedicated team. You will perform site visits, help recruit patients, and ensure compliance with GCP and ICH guidelines across diverse therapeutic areas.

Ideal candidates hold a university degree in science or health care, have experience in pharma or clinical trials, strong MS Office skills, and fluency in Spanish and English. Travel flexibility and a valid driving license are required.

Formación

  • University degree in scientific discipline or health care.
  • Experience in Pharma Industry, and/or Clinical Trials environment.
  • Very good computer skills including MS Office.
  • Excellent command of Spanish and English language.
  • Organizational, time management and problem-solving skills.
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
  • Flexibility to travel.
  • Driver’s license class B.

Responsabilidades

  • Performing site selection, initiation, monitoring and close-out visits.
  • Supporting the development of a subject recruitment plan.
  • Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and ICH guidelines.
  • Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions.
  • Collaborating with experts at study sites and with client representatives.

Conocimientos

MS Office
Spanish
English
Organizational skills
Time management
Problem solving
Travel flexibility
Driver’s license

Educación

University degree in scientific discipline or health care

Herramientas

MS Office

Descripción del empleo

IQVIA Spain in Barcelona is seeking a Clinical Research Associate to join our Sponsor dedicated team. You will perform site visits, help recruit patients, and ensure compliance with GCP and ICH guidelines across diverse therapeutic areas.

Ideal candidates hold a university degree in science or health care, have experience in pharma or clinical trials, strong MS Office skills, and fluency in Spanish and English. Travel flexibility and a valid driving license are required.

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