298 offres d'emploi Clinical Trial Manager - |
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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 :
Société : Chronos Consulting
The role is % remote with up to 40% travel and based in Europe.As part of the global clinical affairs team,..hands-on manager with experience in managing Core Labs,..
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Société : Chronos Consulting
sites and vendors required for conduct of clinical trialsDirect/Manage necessary clinical trial approvals from IRBs/ECs,..
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Lieu :
Société : Chronos Consulting
country) conform to Good Clinical Practice regulations and standardsEnsure adherence to protocols and compliance with regulatory (FDA/ICH/ISO/GCP) guidelines as well as SOP proceduresIdentify clinical training needs and develop training materials for in-house and clinical<..
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Lieu :
Société : Chronos Consulting
country) conform to Good Clinical Practice regulations and standardsEnsure adherence to protocols and compliance with regulatory (FDA/ICH/ISO/GCP) guidelines as well as SOP proceduresIdentify clinical training needs and develop training materials for in-house and clinical<..
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Lieu :
Société : Chronos Consulting
The role is % remote with up to 40% travel and based in Europe.As part of the global clinical affairs team,..take corrective actions where necessary to address issuesDevelops budget for all clinical projects and adhere to company financial goalsEnsure clinical results ..
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Lieu :
Société : Chronos Consulting
Biopharmaceutical experience would provide a strong advantage3) Additional 4+ years direct experience in clinical trial management4) Solid track record in successfully executing Phase I – III clinical trials5) Demonstrated expert knowledge and comprehensive un..
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Lieu :
Société : Chronos Consulting
country) conform to Good Clinical Practice regulations and standardsEnsure adherence to protocols and compliance with regulatory (FDA/ICH/ISO/GCP) guidelines as well as SOP proceduresIdentify clinical training needs and develop training materials for in-house and clinical<..
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Lieu :
Société : Chronos Consulting
country) conform to Good Clinical Practice regulations and standardsEnsure adherence to protocols and compliance with regulatory (FDA/ICH/ISO/GCP) guidelines as well as SOP proceduresIdentify clinical training needs and develop training materials for in-house and clinical<..
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Lieu : Brussels Brussels
Société : IQVIA
to the Clinical Program Lead (CPL)Resourcing and training of Functional Service Provider (FSP) CRAs for assigned study(ies) Validating local CRO resources,..
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Lieu : Brussels Brussels
Société : IQVIA
technology solutions and clinical research services to the life sciences industry...standardize processes across the studies to improve efficiencies in CO activitiesDefine monitoring requirements including components of Risk Based Monitoring (RBM)Support risk management and signal d..
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Lieu : Brussels Brussels
Société : IQVIA
to the Clinical Program Lead (CPL)Resourcing and training of Functional Service Provider (FSP) CRAs for assigned study(ies) Validating local CRO resources,..
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Lieu : Brussels Brussels
Société : IQVIA
PharmD) is preferred.8+ years of clinical research experience in biopharma or CRO4+ years of clinical project management wit regional or global scopeDemonstrated project management skills across multiple highly complex clinical studiesExperience of managing multiple st..
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Lieu : Ghent Flanders
Société : Argenx
clear way and energizes and motivates the CDT team members as well as the respective CTMs to work towards achieving the clinical goals in line with the OGSM and argenx’ cultural pillars.If applicable,..
Postuler | Plus d'offres Clinical Operations Development Lead
Plus d'offres - Ghent |
Lieu : Ghent Flanders
Société : Argenx
issues/risks and financial status.Ensures audit/inspection readiness of the assigned program/trials...the CODL co-leads the Clinical Development Team (CDT) and co-owns the Clinical Development Plan (CDP).As ad-hoc member of the Asset Strategy Team (AST),..
Postuler | Plus d'offres Clinical Operations Development Lead
Plus d'offres - Ghent |
Lieu : Ghent Flanders
Société : Argenx
acts as line manager of CTMs and/or CTAs:Interviewing candidatesOn-boarding of new direct reportsEnsuring that assigned staff are trainedGoal setting and reviewMentoring and enabling the growth and development of assigned staffSupports ClinOps and Global Company initiatives as appli..
Postuler | Plus d'offres Clinical Operations Development Lead
Plus d'offres - Ghent |
Lieu : Ghent Flanders
Société : Argenx
the CODL drives the execution of the clinical program in collaboration with the CDT members and according to what is in the CDP.The CODL oversees the clinical trial budgets,..
Postuler | Plus d'offres Clinical Operations Development Lead
Plus d'offres - Ghent |
Lieu : Ghent Flanders
Société : Argenx
after completion of the Clinical Phase III program,..The CDT is responsible for the clinical development strategy,..
Postuler | Plus d'offres Clinical Operations Development Lead
Plus d'offres - Ghent |
Lieu :
Société : Keyrus Life Science
ensuring that clinical trial specifics needs are met...you can count on us to support you at each step of your project thanks to regular touch points with our Key Account Manager. We then also carefully choose with you what would be your next assignment that is matchi..
Postuler | Plus d'offres Clinical Supply Partnering Associate |
Lieu : Brussels Brussels
Société : Proclinical
- Act as line manager of Clinical Trial Managers (CTMs) and/or Clinical Trial Associates (CTAs).Requirements:..
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Lieu : Brussels Brussels
Société : Proclinical
- Accountable for all clinical-related aspects within the assigned therapeutic indication/program...- Proven Clinical Operations experience in a relevant global leadership position in the pharmaceutical/biotech industry...
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Lieu : Brussels Brussels
Société : Proclinical
The Clinical Operations Program Directors co-leads the Clinical Development department and co-owns the Clinical Development Plan...
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Lieu : Brussels Brussels
Société : Proclinical
- Lead the Clinical Development meetings,......As a result,..- Oversee the clinical trial budgets,..
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Lieu : Zaventem Flanders
Société : Zoetis
and retrainBe an expert on your solutions – know them inside and out,..transparentie register,..She/he monitors compliance of artwork,..
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Lieu : Zaventem Flanders
Société : Zoetis
Associate Manager / Manager.JOB PURPOSE:In collaboration with the RA team members,..audits/inspections support…).The RA&C Associate-Mgr / Mgr needs to have/acquire expertise in National/EU Regulatory legislations (including the NVR) for medicines and other Zoetis types of r..
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