Research Associate Jobs in Bucharest

Here at Fortrea we are recruiting a junior Clinical Research Associate I to work within our multisponsor clinical team.Key ResponsibilitiesConduct site monitoring activities including prestudy initiation routine monitoring and closeout visits.Ensure patient safety data integrity and protocol complia...

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...

Considered as the Primary Sponsor Point of contact for the investigative site.  Advanced level of competency or experience in providing contextual information on the clinical trials connecting stakeholders to the investigative sites and strengthening Abbvies positioning.  Ability to motivate and ali...

Manage deliver and/or perform full clinical site monitoring services for one or more projects which may include multiple services be complex in nature and/or run on a multinational -house based position responsible for the design and oversight of project monitoring services including training site/p...

Manage deliver and/or perform full clinical site monitoring services for one or more projects which may include multiple services be complex in nature and/or run on a multinational -house based position responsible for the design and oversight of project monitoring services including training site/p...

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan Protocol Good Clinical Practice (GCP) ICH guidelines and l...

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan Protocol Good Clinical Practice (GCP) ICH guidelines and l...

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan Protocol Good Clinical Practice (GCP) ICH guidelines and l...