We are seeking a Clinical Researcher to join the Diabetes and Metabolism Research Group
Main responsibilities and duties:
- Participate as a Sub-Investigator in clinical trials in obesity.
- Perform medical visits related to the clinical trials in obesity, as per protocol: patient´s recruitment, informed consent sign, physical examination, medical history, treatment adjustment, adverse events, serious adverse events, etc) under the supervision of the PI and study team.
- Collaborate closely with the medical team, study coordinators and other departments involved in the clinical trials.
- Monitor and follow up participants throughout the clinical trial, ensuring appropriate clinical follow-up and compliance with study procedures.
- Contribute to other research activities within the research group, as agreed with the Principal Investigator.
- Participate, where appropriate, in national and international scientific meetings and other activities of the research group
Education and qualifications:
Required:
- Holds a degree in Medicine
- Completion of specialist training (MIR)
- MIR speciality in Endocrinology and Nutrition, Internal Medicine or Clinical Pharmacology
Desirable:
- Additional training in data management, data bases and statistics
- Additional training in Clinical Trials
- Additional training in obesity clinical management
Experience and knowledge:
Required:
- Experience:
- Relevant clinical experience as a medically qualified professional.
- Experience in participation in research lines and/or projects.
- At least 1 year of experience working as clinical investigator in clinical trials.
- Knowledge of Good Clinical Practice.
- Ability to work in a multidisciplinary team
Note: Applicants may be required to provide evidence of their experience and achievements related to the requirements of the position during the application process through the ATS.
Desirable:
- Knowledge on how to manage electronic medical history registry: ARGOS, SAP.
- Knowledge of e-CRF and management of clinical data related to clinical trials
Labour conditions:
- Working hours : Part-time (10 hours per week).
- Starting date : As soon as possible.
- Gross annual salary : €12,000
- Contract type : Technical and scientific activities contract linked to project activities
What can we offer?
- Incorporation into the Vall d’Hebron Research Institute (VHIR) , a public sector institution that promotes and develops biomedical research, innovation and teaching at Vall d’Hebron University Hospital (HUVH), the largest hospital in Barcelona and the largest within the Catalan Institute of Health (ICS) .
- A dynamic scientific environment of excellence , where cutting-edge biomedical projects are continuously developed.
- Continuous learning and career development pathways .
- Flexible working hours .
- 23 days of annual leave plus 9 personal days .
- Adaptable remuneration programme , including meal vouchers, health insurance, transport and more.
- Corporate benefits platform , offering significant discounts on travel, culture, technology, gastronomy, sports and more.
- Healthy offering– “Feel Good, Feel VHIR” : VHIR’s wellbeing programme offers a variety of activities to help staff thrive—physically, mentally, and socially. Through four pillars—Feel Well, Feel Connected, Feel Empowered, Feel Welcomed—it fosters health, growth, and community.
- International mobility support (Welcome Services) : we aim to make your arrival in Barcelona smooth and pleasant by providing city information, guidance on required procedures, access to the International Welcome Desk, family support and assistance with finding accommodation.
Deadline to apply: 16-11-2026
How We Hire:
Pre-selection: Candidates are shortlisted based on their skills, qualifications, and relevant experience as outlined in their CVs.
Interviews: Meetings may be held with Talent Acquisition and/or the hiring manager.
Practical assessment: Depending on the role, candidates may complete a case study, te
📌 Clinical Researcher (España)
🏢 VHIR
📍 España