Pediatric Clinical Research Physician (Part-Time)

Fundació Hospital Universitari Vall d'Hebron- Institut de recerca

España

Sur place

EUR 24 000 - 36 000

Temps partiel

Il y a 10 jours

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Avantages offerts par ce poste

23 days annual leave
9 personal days
Meal vouchers
Health insurance
Transport benefits
Wellbeing programme

Résumé du poste

Fundació Hospital Universitari Vall d’Hebron- Institut de recerca seeks a Clinical Researcher to join the Paediatric Endocrinology Unit. The role is part‑time (16 h/week) with hospital clinical trial oversight, coordinating visits and protocol assessments in paediatric endocrinology.

The candidate will work with principal investigators, study coordinators and the Clinical Trials Unit, contributing to protocol development, data collection and publications.

Qualifications

  • Experience in clinical trials in paediatric endocrinology.
  • More than 5 years of clinical experience in hospital paediatrics.
  • Working knowledge of regulatory framework for clinical trials in paediatric population.
  • Good Clinical Practice (ICH‑GCP) certification or commitment to obtain.
  • Languages: Spanish and English (business level).
  • Postgraduate training in clinical research methodology, biostatistics or pharmacovigilance.

Responsabilités

  • Conduct of clinical trial visits in paediatric endocrinology under PI supervision.
  • Assess eligibility and manage informed consent/assent.
  • Record adverse events and review concomitant medications.
  • Complete source data documentation and eCRF entries.
  • Coordinate with sponsors, CRO monitors, Pharmacy and CTU.
  • Support investigator‑initiated research and publications.
  • Follow‑up on CF‑related endocrine complications with CF unit.

Description du poste

Fundació Hospital Universitari Vall d’Hebron- Institut de recerca seeks a Clinical Researcher to join the Paediatric Endocrinology Unit. The role is part‑time (16 h/week) with hospital clinical trial oversight, coordinating visits and protocol assessments in paediatric endocrinology.

The candidate will work with principal investigators, study coordinators and the Clinical Trials Unit, contributing to protocol development, data collection and publications.

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