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
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
Reporting to the Clinical Operations Manager,..Quality Assurance: Review applicable clinical study plans and create or support the development of a Trial Master File plan for each clinical study...
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
focusing on the essential documents as per ISO14155 and Good Clinical Practice (GCP) guidelines...Capacity to work effectively with project managers,..
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 :
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
etc.)Keys to Success:Education:MS/PhD – minimum of 3 years of proven experienceBS/Nurse – minimum of 5 years of proven experienceExtensive global clinical trial/study management experienceWorking knowledge of Good Clinical Practices,..
Postuler |
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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..
Postuler |
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 : 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
review and validation of the clinical data promptly;..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 clinica..
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 : Zaventem Flanders
Société : IQVIA
services will ensure the local trial team is delivering quality data and trial documents/records that are compliant with the assigned clinical trial protocol,..
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
..review and validation of the clinical data promptly;..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 ..
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 : 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 : 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
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 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
and supply planning of clinical trials.Experience working with global regulatory requirements,..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
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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