298 offres d'emploi Clinical Trial Manager - |
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Lieu : Leuven Flanders Société : Terumo Job Responsibilities As a Clinical Trial Assistant,..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 Ability to work with electronic Trial Master Files (eTMF),..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 Reporting to the Clinical Operations Manager,..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 Ability to work with electronic Trial Master Files (eTMF),..you will be an essential part of our dynamic European Medical and Clinical Division at the EMEA HQ...
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...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 Join our team as a Clinical Trial Assistant and play a pivotal role in advancing medical research...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 : 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 digital and decentralized clinical trial services...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 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,..
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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 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 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 Manageme..
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...codes of Good Clinical Practice (GCP),..
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 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 : 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 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,..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 : Rixensart Wallonia Société : 1054 GlaxoSmithKline Services Unlimited The SCM is accountable for determining supply strategies that successfully deliver investigational medicines to patients while ensuring the supply chain delivers results that support GSK R&D registration & launch milestones.The SCM is responsible for influencing clinical plans relat..
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 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 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 ICH and GCPs.Experience working with senior leadership including but not limited to Clinical Operations,..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 |
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