Research Associate Jobs in Barcelona

Research AssociateResearch Associates (RAs) are expected to manage either one major data collection project or up to two minor data collection projects within a given period. Each RA reports functionally to the Project Manager (PM) overseeing the data collection cycle.Key Responsibilities: Support t...

Vall dHebron Research Institute (VHIR) is a public sector institution located in Barcelona (Spain) that promotes and develops innovative biomedical research at the University Hospital Vall dHebron. VHIR is oriented towards finding solutions to the health problems of the citizens and has the will to...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionLocations we are hiring:Barcelona and Seville onlyJoin Us as an Assistant Clinical Research Associate Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more...

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...

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...

This is what you will do: The Associate Director Global Health Economics and Outcomes Research Innovation (GHEOR) is a strategic pharmaceutical/biotech leader who bridges product development with health economics evidence generation and outcomes assessments and novel capabilities (including generati...

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...