Clinical Trials Coordinator — Neuromuscular Disorders Lab

Vall d'Hebron Institute of Research (VHIR)

Barcelona

In loco

EUR 26.000 - 29.000

Tempo pieno

6 giorni fa
Candidati tra i primi
Generatore di candidature

Distinguiti per questa posizione — genera un curriculum e una lettera di presentazione personalizzati in circa un minuto.

Supera i filtri ATS

Vantaggi offerti da questo lavoro

Flexible working hours
Meal vouchers
Health insurance
Transport benefits
Wellbeing program

Descrizione del lavoro

Vall d’Hebron Institute of Research (VHIR) seeks a Study Coordinator specialised in neuromuscular diseases to join the Peripheral Nervous System Research Group in Barcelona. The role coordinates clinical trials, manages patient visits and ensures quality data entry, under GCP guidelines.

The ideal candidate has a Biosciences degree, fluency in Catalan, Spanish and English, and at least 1 year of study coordination experience. A Master in Clinical Trials is desirable.

Competenze

  • Experience working in clinical trials.
  • At least 1 year of experience working as Study Coordinator.

Mansioni

  • Coordinate and manage clinical trials in collaboration with Investigators and the clinical research team.
  • Coordinate patient visits, study procedures and follow-up throughout the clinical trial.
  • Ensure accurate and timely completion of study documentation and data entry.
  • Coordinate communication with patients, sponsors, monitors and other stakeholders.
  • Ensure compliance with study protocols, Good Clinical Practice (GCP) and applicable regulations.

Conoscenze

Clinical trials experience
Study coordination
Multilingual (Catalan/Spanish/English)

Formazione

Bachelor’s Degree in Biosciences
Master in Clinical Trials

Descrizione del lavoro

Vall d’Hebron Institute of Research (VHIR) seeks a Study Coordinator specialised in neuromuscular diseases to join the Peripheral Nervous System Research Group in Barcelona. The role coordinates clinical trials, manages patient visits and ensures quality data entry, under GCP guidelines.

The ideal candidate has a Biosciences degree, fluency in Catalan, Spanish and English, and at least 1 year of study coordination experience. A Master in Clinical Trials is desirable.

Ottieni la revisione del curriculum gratis e riservata.

o trascina qui il file.

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