8 offres d'emploi Preclinical Science and Operations lead (Oncology) Human Health - be |
|
Site source : Talent BE Lieu : Charleroi Wallonia Société : Univercells Détail de l'offre : drives projects to plan.* Ensures that GLP requirements for study related documentation are met.* Acts as subject matter expert on in vivo operations.* Ensures all studies are conducted to the highest bioethical standards….REQUIREMENTS & QUALIFICATIONS:* Relevant academic qualific..
Postuler |
Site source : Talent BE Lieu : Charleroi Wallonia Société : Univercells Détail de l'offre : Animal Science Lead,..ideally in the area vaccines and oncology* Knowledge of GLP or GLP-trained or at least experience with Good Research Practices (GRP) for studydocumentation.* Good communication skills.* Effective collaborator.* Analytical skills.* Fluency in Engli..
Postuler |
Site source : Talent BE Lieu : Charleroi Wallonia Société : Univercells Détail de l'offre : characterization and mitigation.o Issue management and resolution.o Contingency planning.* Designs study operations and ensures appropriate documentation is prepared.* Ensures the viability of the analysis plan and contributes to planning and analysis.* Drives operational budgets an..
Postuler |
Site source : Talent BE Lieu : Charleroi Wallonia Société : Univercells Détail de l'offre : characterization and mitigation.o Issue management and resolution.o Contingency planning.* Designs study operations and ensures appropriate documentation is prepared.* Ensures the viability of the analysis plan and contributes to planning and analysis.* Drives operational budgets an..
Postuler |
Site source : Talent BE Lieu : Brussels Brussels Société : IQVIA Détail de l'offre : Liaison between Country Operations (CO) teams and the Global Study Team:..technology solutions and clinical research services to the life sciences industry...
Postuler |
Site source : Talent BE Lieu : Brussels Brussels Société : IQVIA Détail de l'offre : 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 detection at a study levelAct as a Subject Matter Expert for Sponsor Inspections by Regulato..
Postuler |
Site source : Talent BE Lieu : Brussels Brussels Société : IQVIA Détail de l'offre : 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 studies including exten..
Postuler |
Site source : Talent BE Lieu : Brussels Brussels Société : IQVIA Détail de l'offre : to support execution of the study(ies)Developing and/or reviewing applicable study documents including training materials and reportsDelivery of appropriate protocol and indication training to Country Operations teamsCoordinationof start up and recruitment activities at the study le..
Postuler |
|