Clinical Researcher (España)

Clinical Researcher (España)

19 oct
|
Fundacio Hospital Universitari Vall d'Hebron- Institut de recerca
|
España

19 oct

Fundacio Hospital Universitari Vall d'Hebron- Institut de recerca

España

Organisation/Company Fundació Hospital Universitari Vall d'Hebron- Institut de recerca Department Research Department Research Field Biological sciences » Biology Researcher Profile Other Profession Positions Other Positions Application Deadline 18 Oct 2026 - 23:59 (Europe/Andorra) Country Spain Type of Contract Temporary Job Status Part-time Hours Per Week 16h/week Is the job funded through the EU Research Framework Programme? Other EU programme Is the Job related to staff position within a Research Infrastructure? No
Offer Description
The Paediatric Endocrinology Unit of Vall d’Hebron University Hospital is a tertiary referral unit covering the whole spectrum of paediatric endocrine disease, and works closely with the Growth and Development research group of the Vall d’Hebron Research Institute (VHIR). The Unit runs an active portfolio of clinical trials in paediatric endocrinology, with a particular focus on growth disorders, obesity and metabolic disease in children and adolescents.




We are seeking a Clinical Researcher for a paediatrician position with hospital clinical experience and a background in clinical trials to join the Unit on a part‑time basis (16 h/week) as a clinical research physician. The successful candidate will run trial visits and protocol‑driven assessments in close collaboration with the principal investigators, the study coordinators and the hospital’s Clinical Trials Unit.
Main responsibilities and duties:
- Conduct of clinical trial visits in paediatric endocrinology (screening, inclusion, follow‑up and end of study) under the supervision of the principal investigator.
- Assessment of eligibility criteria and management of the informed consent and assent process with patients and their legal guardians.
- Protocol-driven clinical assessments, recording and reporting of adverse events, and review of concomitant medication.
- Source data documentation, eCRF completion and resolution of queries.
- Coordination with sponsors, CRO monitors, Hosp

📌 Clinical Researcher (España)
🏢 Fundacio Hospital Universitari Vall d'Hebron- Institut de recerca
📍 España

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