Study Coordinator, Epilepsy Trials (Flexible Hours)

Vall d’Hebron Institute of Research (VHIR) - Vall d'Hebron Institut de Recerca; Barcelona; On-site; EUR 22,000 - 26,000; Full time

Benefits offered by this job

Meal vouchers

Health insurance

Transport

Flexible remuneration

23 days annual leave

9 personal days

Corporate benefits platform

International mobility support

Job summary

The Vall d’Hebron Institute of Research (VHIR) in Barcelona invites applications for a study coordinator to support the Epilepsy Team across multiple research projects. You will help plan and execute studies, manage data, and assist in clinical trial coordination, reporting, and regulatory tasks.

Required: Bachelor’s in Health Sciences or equivalent, high English level (C1), fluency in Catalan/Spanish, and a Good Clinical Practice certificate. Desirable: Master’s in Clinical Trials.

Qualifications

• Bachelor’s degree in Health Sciences or equivalent.
• High level of English language (C1).
• Fluency in Catalan and Spanish.
• Good clinical practice certificate.
• Good knowledge of neurological disorders.
• Good written and verbal communication skills.
• Ability to work independently as well as in a team.

Responsibilities

• Provide support to the research team in planning and implementation of studies.
• Perform data management tasks ensuring data accuracy and quality.
• Support coordination and management of clinical trials and projects.
• Provide technical and operational support to the Epilepsy Team.

Skills

English (C1)

Communication skills

Independent work

Team collaboration

Organization

Self-motivation

Education

Bachelor’s degree in Health Sciences or equivalent

Master’s degree in Clinical Trials or similar

Tools

REDCap

SAP management program

Job description

The Vall d’Hebron Institute of Research (VHIR) in Barcelona invites applications for a study coordinator to support the Epilepsy Team across multiple research projects. You will help plan and execute studies, manage data, and assist in clinical trial coordination, reporting, and regulatory tasks.

Required: Bachelor’s in Health Sciences or equivalent, high English level (C1), fluency in Catalan/Spanish, and a Good Clinical Practice certificate. Desirable: Master’s in Clinical Trials.