298 offres d'emploi Clinical Trial Manager - |
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Lieu : Leuven Flanders
Société : Terumo
Reporting to the Clinical Operations Manager,..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...ensuring the success of clinical studies...
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...Reporting to the Clinical Operations Manager,..
Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven |
Lieu : Leuven Flanders
Société : Terumo
Capacity to work effectively with project managers,..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
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
you'll be at the forefront of clinical research excellence,..Reporting to the Clinical Operations Manager,..
Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven |
Lieu :
Société : Thermo Fisher Scientific
and assessing site activation plansLeads study risk planning process in context of site and subjectCoordinate study/protocol training & investigator meetingsDevelops and provides key inputs to Clinical Trial BudgetLeads inspection readiness activities related to study managem..
Postuler |
Lieu :
Société : Thermo Fisher Scientific
may be required to act as ‘lead’ study manager,..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 Researc..
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Lieu :
Société : Thermo Fisher Scientific
reviewing Pre-trial Assessment outputs,..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 a..
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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,..
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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
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
..technology solutions and clinical research services to the life sciences industry...if delegated by FM.Ensure accurate finance reporting and trial delivered within budgetKeeps the trial in compliance with local regulatory requirements by organizing and ensuring IEC/H..
Postuler | Plus d'offres Clinical Project Manager
Plus d'offres - Zaventem |
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 : 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
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
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
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 : 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
ICH and GCPs.Experience working with senior leadership including but not limited to Clinical Operations,..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
and CMC leadership.Project management experiencePreferred Qualifications:Understanding of the drug development process and experience with clinical supplies manufacturing and packagingAbility to maintain accurate records and files in accordance with cGMPs and SOPs.Ability to indepen..
Postuler | Plus d'offres Clinical Supply Chain Manager
Plus d'offres - Rixensart |
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
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 |
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