24-03-2026

Health Technician (Degree in the field of Health Sciences (Human Nutrition and Dietetics, Nursing, Psychology, Pharmacy, Biology, Biomedicine or related degrees). Postgraduate or master's training related to the clinical field will be valued.).

Ref.:

FIMIM3205-DE LA TORRE

Institution:

FUNDACIÓ IMIM

Researcher/s responsible for the project:

Rafael De La Torre Fornell

Project title:

Phase IIa clinical trial of an innovative therapy for Fragile X Syndrome patients (CPP2022-009659)

Research group / Service:

Integrative pharmacology and systems neuroscience research group

Description:

The selected person will join the Integrative pharmacology and systems neuroscience research group (Neurosciences research program).

Task:

To support the follow-up of volunteers participating in the clinical study "Phase IIa clinical trial of an innovative therapy for patients with Fragile X Syndrome", including the logistical management of visits, preparation of materials and organization of agendas.

Formation:

Bachelor's degree in the field of Health Sciences (Human Nutrition and Dietetics, Nursing, Psychology, Pharmacy, Biology, Biomedicine or related qualifications). Postgraduate or master's degree training related to the clinical field will be valued.

Experience:

- Experience in clinical research studies, preferably in clinical trials with the participation of volunteers or patients. - Experience in managing and monitoring participants in research projects (coordination of visits, contact with participants, recruitment support and longitudinal monitoring). -Experience in logistical management of clinical studies, including organization of agendas, preparation of study materials and support to the research team. - Experience in the introduction and management of research data (CRD/eCRF or study databases). -Previous experience in health intervention projects or clinical trials and knowledge of clinical research procedures will be positively valued.

Knowledge:

- Knowledge of common office automation software (Excel, Word, PowerPoint) and clinical management tools (SAP, Citrix, PCN or similar). - Knowledge of clinical research procedures and protocols, including visit management, participant follow-up, and study data entry. - Experience in database management or study platforms (CRD/eCRF). - Good command of Catalan and Spanish; Knowledge of scientific English will be valued.

Additional information:

The following will be especially valued: -Ability to organize and plan. -Autonomy in the management of tasks and monitoring of studies. -Ability to work in multidisciplinary clinical research teams. The cost of the contract is subsidized by the State Research Agency.

Contract:

Duració determinada vinculat a programes finançats amb fons europeus (PRTR) 12p

Schedule	Retribution	Hire date
Full time	31428.32 € bruts anuals	April 2026