298 offres d'emploi Clinical Trial Manager - |
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Lieu : Leuven Flanders
Société : Terumo
Collaboration: Establish and maintain strong collaborative relationships with investigation site personnel and Clinical Research Associates (CRAs) to ensure the completeness of the Trial Master File...
Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven |
Lieu : Leuven Flanders
Société : Terumo
Investigator Site File (ISF): Prepare the ISF during the activation phase of clinical studies,..Reporting to the Clinical Operations Manager,..
Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven |
Lieu : Leuven Flanders
Société : Terumo
..Ability to work with electronic Trial Master Files (eTMF),..Capacity to work effectively with project managers,..
Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven |
Lieu : Leuven Flanders
Société : Terumo
Reporting to the Clinical Operations Manager,..you'll have the opportunity to engage in meaningful conversations with the hiring manager and other enthusiastic Terumo associates...
Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven |
Lieu : Leuven Flanders
Société : Terumo
Job Responsibilities As a Clinical Trial Assistant,..Profile Description Prior experience in clinical trial administration is essential...
Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven |
Lieu : Leuven Flanders
Société : Terumo
Join our team as a Clinical Trial Assistant and play a pivotal role in advancing medical research...Ability to work with electronic Trial Master Files (eTMF),..
Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven |
Lieu :
Société : Thermo Fisher Scientific
may be required to act as ‘lead’ study manager,..reviewing Pre-trial Assessment outputs,..With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portf..
Postuler |
Lieu :
Société : Thermo Fisher Scientific
The Study Manager has global responsibility for one or more studies of moderate complexity generally with responsibility for all study management aspects of assigned studiesProvides quality oversight to the Contract Research Organization (CRO) and of the CRO deliverables related to ..
Postuler |
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Lieu :
Société : Thermo Fisher Scientific
The Study Manager has global responsibility for one or more studies of moderate complexity generally with responsibility for all study management aspects of assigned studiesProvides quality oversight to the Contract Research Organization (CRO) and of the CRO deliverables related to ..
Postuler |
Lieu :
Société : Thermo Fisher Scientific
With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio,..
Postuler |
Lieu : Bruxelles Brussels
Société : EORTC
with the close coaching of a Clinical Data Expert:Clinical trial protocolDevelopment of the Data Management sections of the clinical trial protocolAssisting in the final review of the clinical trial protocol for consistency and operational f..
Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles |
Lieu : Bruxelles Brussels
Société : EORTC
data cleaning and data reporting activitiesApplication of QC to each stage in the data handling to ensure the data are reliable and processed in compliance with ICH-GCP requirements.Communication with the participating investigators to resolve queries and collect missing dataPerforming the..
Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles |
Lieu : Bruxelles Brussels
Société : EORTC
Share onThe Clinical Data Manager works under the hierarchical supervision of the Clinical Data Expert...
Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles |
Lieu : Zaventem Flanders
Société : IQVIA
etc.Complies with relevant training requirements.Contribute to quality Site SelectionEnsures local/country team is meeting recruitment targets with high quality data on time and within study budgetAct as primary contact for assigned trial at the country level,..
Postuler | Plus d'offres Clinical Project Manager
Plus d'offres - Zaventem |
Lieu : Bruxelles Brussels
Société : EORTC
data cleaning and data reporting activitiesApplication of QC to each stage in the data handling to ensure the data are reliable and processed in compliance with ICH-GCP requirements.Communication with the participating investigators to resolve queries and collect missing dataPerforming the..
Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles |
Lieu : Bruxelles Brussels
Société : EORTC
Share onThe Clinical Data Manager works under the hierarchical supervision of the Clinical Data Expert...
Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles |
Lieu : Bruxelles Brussels
Société : EORTC
Share onThe Clinical Data Manager works under the hierarchical supervision of the Clinical Data Expert...
Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles |
Lieu : Bruxelles Brussels
Société : EORTC
data cleaning and data reporting activitiesApplication of QC to each stage in the data handling to ensure the data are reliable and processed in compliance with ICH-GCP requirements.Communication with the participating investigators to resolve queries and collect missing dataPerforming the..
Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles |
Lieu : Bruxelles Brussels
Société : EORTC
The Clinical Data Manager reports on study activities and status to the study team.The Clinical Data Manager is responsible for all the steps required for the setup of the Data Management tools of a clinical trial and for the collection,..
Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles |
Lieu : Bruxelles Brussels
Société : EORTC
The Clinical Data Manager reports on study activities and status to the study team.The Clinical Data Manager is responsible for all the steps required for the setup of the Data Management tools of a clinical trial and for the collection,..
Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles |
Lieu : Rixensart Wallonia
Société : 1054 GlaxoSmithKline Services Unlimited
We are seeking a highly motivated Clinical Supply Chain Manager that thrives in a fast-paced and dynamic environment while working on multi-disciplinary teams...
Postuler | Plus d'offres Clinical Supply Chain Manager
Plus d'offres - Rixensart |
Lieu : Rixensart Wallonia
Société : 1054 GlaxoSmithKline Services Unlimited
The Supply Chain Manager (SCM) role provides strategic oversight of the end-to-end supply chain for assigned GSK R&D investigational assets...
Postuler | Plus d'offres Clinical Supply Chain Manager
Plus d'offres - Rixensart |
Lieu : Rixensart Wallonia
Société : 1054 GlaxoSmithKline Services Unlimited
This role supports Phase I through IV GSK sponsored clinical studies as well as investigator sponsored trials and compassionate use programs.Leads the cross-functional Clinical Supply Chain Network team and is accountable for the Clinical Supply Workstream as pa..
Postuler | Plus d'offres Clinical Supply Chain Manager
Plus d'offres - Rixensart |
Lieu : Rixensart Wallonia
Société : 1054 GlaxoSmithKline Services Unlimited
and procedures5+ years of experience working in pharmaceuticals.Experience in the management of clinical trial supplies including,..
Postuler | Plus d'offres Clinical Supply Chain Manager
Plus d'offres - Rixensart |
Lieu : Rixensart Wallonia
Société : 1054 GlaxoSmithKline Services Unlimited
..ICH and GCPs.Experience working with senior leadership including but not limited to Clinical Operations,..The SCM is accountable for determining supply strategies that successfully deliver investigational medicines to patients while ensuring the supply chain delivers results that ..
Postuler | Plus d'offres Clinical Supply Chain Manager
Plus d'offres - Rixensart |
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