Clinical Trials Study Coordinator

FUNDACION INSTITUTO INVESTIGACION SANITARIA FUNDACION JIMENEZ DIAZ

España

Presencial

EUR 28.000 - 42.000

Jornada completa

Hace 7 días
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Descripción de la vacante

FUNDACION INSTITUTO INVESTIGACION SANITARIA FUNDACION JIMENEZ DIAZ invites applications for a Study Coordinator/Clinical Trial Coordinator to oversee the conduct of clinical trials, ensure protocol adherence, and coordinate trial activities with investigators, monitors, sponsors, and study teams.

The role involves managing trial documentation, scheduling patient visits, data entry support for electronic CRFs, and maintaining regulatory files, with emphasis on proactive problem solving, teamwork,

Formación

  • Requires university degree in a relevant field.
  • Certificate in Good Clinical Practice (GCP) guidelines – ICH E6(R3).
  • Proactive, self-motivated, and solution-oriented with strong organizational and teamwork skills.

Responsabilidades

  • Thorough knowledge of protocols, tests, and procedures for each trial.
  • Coordination of clinical trials with investigators, patients, monitors, sponsors, etc.
  • Coordination and management of the study and study personnel including related tasks.
  • Maintenance and management of trial-related documentation.
  • Scheduling and coordination of visits for patients enrolled in the study.
  • Review of medical records and addenda to meet sponsor requirements; ensure proper documentation.

Conocimientos

Study coordination
Teamwork
Organizational skills

Educación

University degree in Pharmacy/Biology/Biotechnology/Psychology/Education
GCP Certification (ICH E6(R3))

Descripción del empleo

FUNDACION INSTITUTO INVESTIGACION SANITARIA FUNDACION JIMENEZ DIAZ invites applications for a Study Coordinator/Clinical Trial Coordinator to oversee the conduct of clinical trials, ensure protocol adherence, and coordinate trial activities with investigators, monitors, sponsors, and study teams.

The role involves managing trial documentation, scheduling patient visits, data entry support for electronic CRFs, and maintaining regulatory files, with emphasis on proactive problem solving, teamwork,

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