Research Associate Jobs in Spain

Considered as the primary point of contact for the investigative site. High level of competency or experience in providing contextual information on the clinical trials connects stakeholder to the investigative sites and strengthens AbbVies positioning.Aligns trains and motivates the site staff and...

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...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionPosition: CRA (Level I and Level II)Locations: Spain - Madrid (hybrid/remote) / remote in other locationsJoin Us as a Clinical Research Associate (Level I or Level II) Make an Impact at the Forefront of InnovationWe have su...

Work ScheduleEnvironmental ConditionsJob DescriptionJoin Us as a Clinical Research Associate (Level II) Make an Impact at the Forefront of Innovation. You will be fully dedicated to one of our clients.As part of our global team youll have the opportunity to perform and coordinate all aspects of the...

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...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionLocation: Madrid or Barcelona onlyPosition: Assistant CRAJoin Us as an Assistant Clinical Research Associate Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies an...

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...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthi...

Precision for Medicine is not your typical CRO. We are passionate about supporting professional growth and are proud to share extremely high CRA retention rates compared to industry averages.CRAs join us love their jobs and stay because of the amazing people and enjoyable quality of life. Travel is...

Precision for Medicine is not your typical CRO. We are passionate about supporting professional growth and are proud to share extremely high CRA retention rates compared to industry averages.CRAs join us love their jobs and stay because of the amazing people and enjoyable quality of life. Travel is...

Precision for Medicine is not your typical CRO. We are passionate about supporting professional growth and are proud to share extremely high CRA retention rates compared to industry averages.CRAs join us love their jobs and stay because of the amazing people and enjoyable quality of life. Travel is...

National Travel RequiredPerforms on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the studyIdentifies the investigators and verifies that the investigato...

Wood Mackenzie is the global data and analytics business for the renewables energy and natural resources industries. Enhanced by technology. Enriched by human an ever-changing world companies and governments need reliable and actionable insight to lead the transition to a sustainable future. Thats...

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...