Ux Research Associate Jobs in Barcelona
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Clinical Research Associate Ii Barcelona
Fortrea
Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...
Clinical Research Associate
Vhir
VHIR offers a vacant position within its Academic Research Organisation for a CRA to develop and manage activities of monitoring in clinical research projects.Main responsibilities and duties:Making initial follow-up and closing monitoring visits to the participating sites.Preparation of the visits...
Ux Research Analyst (spain, Remote)
Dataforce By Transperfect
Work Location: Spain (Remote)Work Schedule: Monday Friday during regular business hours; Full-timeEngagement Model: Fixed-term EmploymentEstimated Start Date: Early March 2026Estimated Project Duration: 12 months (extension possible)DataForce by TransPerfect is seeking a UX Research Analyst to supp...
Clinical Research Associate Ii Fsp Model Barcelona
Fortrea
We are seeking aSponsor-Dedicated CRA IIwith solid monitoring experience. If you are eager to make an impact this is your chance!This role is to be based inBarcelonaarea.Key Responsibilities:In this role you willMonitor clinical trial sites to ensure compliance with protocols GCP and regulatory requ...
Clinical Research Associate
Astrazeneca
Introduction to role:This role is based in Barcelona with an on-site commitment of three days a week. Fluency in English is required.As a Clinical Research Associate (CRA) within AstraZenecas Oncology Cell Therapy Clinical Operations you will have local responsibility for the delivery of clinical st...
Clinical Research Associate Ii Fsp Team Barcelona
Fortrea
Summary of Responsibilities:Site management for clinical studies is conducted in accordance with Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and sponsor requirements. This includes verifying that study training records are complete and accurate.Site monitoring...