Clinical Research Associate, IQVIA Jobs

Responsibilities: Perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. If applicable, Clinical...

Clinical Research AssociateIQVIA Bucharest is looking for talented and motivated team member to join our Sponsor dedicated team as junior CRA. At this position you will have the opportunity to put...

Responsibilities: Perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. If applicable, Clinical...

Clinical Research AssociateIQVIA Bucharest is looking for talented and motivated team member to join our Sponsor dedicated team as junior CRA. At this position you will have the opportunity to put...

Job OverviewPerform monitoring and site management work for a variety of protocols, site and therapeutic areas.Qualifications• CRA 0.5FTE + Local PM 0.5FTE• Minimum 1 years of PM experience...

Join IQVIA as a CRA / SrCRA (m/w//d) in our Clinical Site Management department home-based throughout Germany. You will focus on a comprehensive clinical trial management in a variety of...

Senior Clinical Research Associate IQVIA is the Human Data Science Company oriented to drive human health outcomes forward.When you join IQVIA Portugal as a sponsor-dedicated CRA, you'll enjoy the...

3ans d'expérience en suivi; FONCTIONS DE BASE: Participe à la préparation et à l'exécution des essais cliniques de phaseI à IV. Supervise l'avancement des investigations cliniques en...

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and...

Responsibilities: Perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. If applicable, Clinical...

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and...

PURPOSEClinical FSP's business model provides dedicated resources to sponsors to work as part of their team.Performing monitoring and site management work to ensure that sites are conducting the...

Job OverviewPerform monitoring and site management work for a variety of protocols, site and therapeutic areas.Qualifications• CRA 0.5FTE + Local PM 0.5FTE• Minimum 1 years of PM experience...

Join IQVIA as a CRA / SrCRA (m/w//d) in our Clinical Site Management department home-based throughout Germany. You will focus on a comprehensive clinical trial management in a variety of...

Senior Clinical Research Associate IQVIA is the Human Data Science Company oriented to drive human health outcomes forward.When you join IQVIA Portugal as a sponsor-dedicated CRA, you'll enjoy the...

3ans d'expérience en suivi; FONCTIONS DE BASE: Participe à la préparation et à l'exécution des essais cliniques de phaseI à IV. Supervise l'avancement des investigations cliniques en...