Clinical Research Jobs in San Luis
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Cdm User Support Manager
Iqvia
Job OverviewAccountable for delivering user support related to clinical document management processes adoption of TMF and good documentation practices across the business.Drives implementation of CDGM initiatives projects and process improvement activities to enhance clinical document management sys...
Clinical Regional Project Lead
Psi Cro
The Regional Project Lead manages and coordinates activities of project teams in designated countries and ensures consistency of Clinical Operations processes across regions. They ensure meeting study milestones are met by the project team on a country and regional level.Ensures planning implementat...
Operations Specialist 1
Iqvia
Job OverviewReview assess and process Safety data and information across service lines received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines under gui...
Global Events Administrator (cvent Experience)
Iqvia
Job OverviewTheEvents Administrator is a key member of IQVIAs Brand & Creative Studio team. The candidate would be responsible for supporting the Global Events Team in managing their projects.They will report into the Director Global Events and set-up event tools (such as event registration websites...
Global Events Administrator
Iqvia
Job OverviewTheEvents Administrator is a key member of IQVIAs Brand & Creative Studio team. The candidate would be responsible for supporting the Global Events Team in managing their projects.They will report into the Director Global Events and set-up event tools (such as event registration websites...
Clinical Research Associate Ii
Psi Cro
If you are currently a CRA I looking forward to the next step of your career this might be the right position for you!As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the highest quality...
Clinical Research Associate I
Psi Cro
Hybrid position in Buenos AiresOnly CVs in English will be consideredWe are looking for a CRA to join our team in Argentina. Here you will have the opportunity to develop yourself as a senior trainer mentor and leader. We are committed to develop our employees in their careers by providing tailored...
Regional Project Lead
Psi Cro
The Regional Project Lead manages and coordinates activities of project teams in designated countries and ensures consistency of Clinical Operations processes across regions. They ensure meeting study milestones are met by the project team on a country and regional level.Ensures planning implementat...
Policy Researcher-senior
European Institute Of Policy Research And Human Rights Sia
The European Institute of Policy Research and Human Rights is a prestigious institution that offers cutting-edge online programs designed to educate future leaders in policy research human rights and related disciplines. Our mission is to deliver world-class skill enhancing programs to candidates gl...
Cluster Executive Medical Director (cemd)
Msd
Job DescriptionCluster Executive Medical Director (CEMD)Division / Area:Global Medical and Scientific AffairsRequired Skills: Accountability Budget Management Business Intelligence (BI) Reporting Clinical Project Management Communication Ethical Standards Healthcare Education Life Cycle Support Mana...
Ihcra I
Fortrea
Job Overview:The In-House Clinical Research Associate (IHCRA I) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the IHCRA I shall reflect their experience and level of contribution which they can ma...
Clinical Data Reviewer
Psi Cro
You will join a widespread yet closely-knit team with the same mentality and desire to develop smart and intelligent approach to project monitoring. You will help to shape the future of effective risk-based monitoring at PSI and ensure higher quality of study data. You will spend time monitoring stu...