298 offres d'emploi Clinical Trial Manager - |
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Lieu : Leuven Flanders
Société : Terumo
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
Sponsor Support: Play a pivotal role in setting up the Trial Master File (TMF)/electronic TMF for the Sponsor,..
Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven |
Lieu : Leuven Flanders
Société : Terumo
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
..you'll be at the forefront of clinical research excellence,..Investigator Site File (ISF): Prepare the ISF during the activation phase of clinical studies,..
Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven |
Lieu : Leuven Flanders
Société : Terumo
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
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 :
Société : Thermo Fisher Scientific
digital and decentralized clinical trial services...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..
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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 :
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..
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Lieu :
Société : Thermo Fisher Scientific
....may be required to act as ‘lead’ study manager,..drive technological innovation and support patients in need...
Postuler |
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,..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 particip..
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
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
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,..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 Manage..
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
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
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
ICH and GCPs.Experience working with senior leadership including but not limited to Clinical Operations,..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
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
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
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 resources/materials,..
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 |
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