298 offres d'emploi Clinical Trial Manager - |
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Lieu : Leuven Flanders
Société : Terumo
Reporting to the Clinical Operations Manager,..Capacity to work effectively with project managers,..
Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven |
Lieu : Leuven Flanders
Société : Terumo
Investigator Site File (ISF):Â Prepare the ISF during the activation phase of clinical studies,..focusing on the essential documents as per ISO14155 and Good Clinical Practice (GCP) guidelines...
Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven |
Lieu : Leuven Flanders
Société : Terumo
Profile Description Prior experience in clinical trial administration is essential...Ability to work with electronic Trial Master Files (eTMF),..
Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven |
Lieu : Leuven Flanders
Société : Terumo
Reporting to the Clinical Operations Manager,..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,..ensuring the success of clinical studies...Ability to work with electronic Trial Master Files (eTMF),..
Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven |
Lieu : Leuven Flanders
Société : Terumo
Capacity to work effectively with project managers,..focusing on the essential documents as per ISO14155 and Good Clinical Practice (GCP) guidelines...
Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven |
Lieu :
Société : Thermo Fisher Scientific
Study Managers may also input to and support compilation of sections to Clinical Study Reports.Will provide leadership to the teams in the setting of realistic recruitment targets and delivery milestones as the single point of accountability for detailed study start-up and mo..
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Lieu :
Société : Thermo Fisher Scientific
Accountable for the development of realistic detailed study startup and monitoring plans as well as study deliveryAccountable for conducting country level feasibility in collaboration with Global Clinical Trial Execution and CROs,..
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Lieu :
Société : Thermo Fisher Scientific
and will coordinate activities of the other Study Managers assigned.A day in the Life:..reviewing Pre-trial Assessment outputs,..
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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 ..
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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
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 : Zaventem Flanders
Société : IQVIA
Site Manager (SM) and Central Trial Manager (CTM)/Global Trial Manager to ensure overall study delivery at the country level.Deliverables:Services rendered will adhere to applicable sponsor’s SOPs,..
Postuler | Plus d'offres Clinical Project Manager
Plus d'offres - Zaventem |
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
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
The Clinical Data Manager will carry out the following tasks,..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 o..
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
review and validation of the clinical data promptly;..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 : Rixensart Wallonia
Société : 1054 GlaxoSmithKline Services Unlimited
ICH and GCPs.Experience working with senior leadership including but not limited to Clinical Operations,..assumptions and constraints of the clinical supply chain and ensures supply options and risks are explored and agreedInfluences team decisions to maximize the use of reso..
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
or related scientific or supply chain discipline.Experience in Upstream and Downstream Clinical Supply Chain processes,..
Postuler | Plus d'offres Clinical Supply Chain Manager
Plus d'offres - Rixensart |
Lieu : Rixensart Wallonia
Société : 1054 GlaxoSmithKline Services Unlimited
to co-ordinate and manage the delivery of clinical supplies for specified GSK asset(s) at the program level.Creates Study Specific Technical Agreements (or equivalent) for specified projects.Accountable for complex problem solving and resolution of issues involving a range of techni..
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 |
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