172 offres d'emploi Associate Director, Study Management - Belgium |
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Site source : Talent BE
Lieu :
Société : Astellas Pharma Inc.
Détail de l'offre : Create and monitor reports on key performance metrics and status of data generation activities aligned with Core Medical Plans and contribute to the strategic implementation of Evidence Generations Plans Lead development of study plans and ensure operational excellence of protocols...
Postuler | Plus d'offres Associate Director, Study Management |
Site source : Talent BE
Lieu :
Société : Astellas Pharma Inc.
Détail de l'offre : managing cross-functional study teams/vendors...Experience of CRO/vendor management and related audits and inspections Strong organizational skills and the ability to prioritize with the ability to navigate change and positively influence others...
Postuler | Plus d'offres Associate Director, Study Management |
Site source : Talent BE
Lieu :
Société : Astellas Pharma Inc.
Détail de l'offre : as part of a continuous improvement ethos you will participate in best-in-class initiatives to improve study execution standards and processes.Hybrid Working:At Astellas we recognize that our employees enjoy having balance between their professional and home lives...
Postuler | Plus d'offres Associate Director, Study Management |
Site source : Talent BE
Lieu :
Société : Astellas Pharma Inc.
Détail de l'offre : Description Associate Director,..Provide oversight and direction to study team members for study deliverables...
Postuler | Plus d'offres Associate Director, Study Management |
Site source : Talent BE
Lieu :
Société : Genmab
Détail de l'offre : complex projects and working with cross-functional teams delivering to project timelines and metrics.Significant experience in project management.Experience working on early and late-stage submissions as per local/regulatory requirements.Equivalent combination of education and exper..
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Site source : Talent BE
Lieu :
Société : Genmab
Détail de l'offre : and clinical data standards development and maintenance.Experience in pharmaceutical industry CDASH/SDTM data standards management and implementation required.Demonstrated experience in all phases of drug development and clinical research in multiple therapeutic areas.Demonstrated k..
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Site source : Talent BE
Lieu :
Société : Genmab
Détail de l'offre : and clinical data standards development and maintenance.Experience in pharmaceutical industry CDASH/SDTM data standards management and implementation required.Demonstrated experience in all phases of drug development and clinical research in multiple therapeutic areas.Demonstrated k..
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Site source : Talent BE
Lieu :
Société : Genmab
Détail de l'offre : data collection and analysis and reporting.Significant Experience in the use of data management systems,..and clinical data standards development and maintenance.Experience in pharmaceutical industry CDASH/SDTM data standards management and implementation required.Demonstrate..
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Site source : Talent BE
Lieu :
Société : Genmab
Détail de l'offre : data collection and analysis and reporting.Significant Experience in the use of data management systems,..CDASH and SDTM mapping and etc. The role provides leadership for the continued development and enforcement of data standards through extensive collaboration with Data Manag..
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Site source : Talent BE
Lieu : Rixensart Wallonia
Société : 1925 GlaxoSmithKline LLC
Détail de l'offre : Project Management,..product incidents) and ensures that risk-reduction strategies are implemented appropriately.Facilitates safety governance/SRTs in the clinical development and post marketing settings by assisting in the establishment and operation of cross-functional teams in an..
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Site source : Talent BE
Lieu : Wavre Wallonia
Société : 1925 GlaxoSmithKline LLC
Détail de l'offre : or a related field.Significant pharmacovigilance experience relating to Safety Evaluation and Risk Management,..Pharmacovigilance Scientists - Associate Director/ Director/ Senior Director Positions in GSK Safety Evaluation and Risk Management (SER..
Postuler |
Site source : Talent BE
Lieu : Rixensart Wallonia
Société : 1925 GlaxoSmithKline LLC
Détail de l'offre : Line Management (including functional matrix reports) leadership competencies include resource and team management,..
Postuler |
Site source : Talent BE
Lieu : Wavre Wallonia
Société : 1925 GlaxoSmithKline LLC
Détail de l'offre : and relations management.If you are passionate about working with colleagues with world-class scientific expertise focused on delivering medicines and devices of significant value for patients and public health,..
Postuler |
Site source : Talent BE
Lieu : Rixensart Wallonia
Société : 1925 GlaxoSmithKline LLC
Détail de l'offre : product incidents) and ensures that risk-reduction strategies are implemented appropriately.Facilitates safety governance/SRTs in the clinical development and post marketing settings by assisting in the establishment and operation of cross-functional teams in any SERM to detect and address..
Postuler |
Site source : Talent BE
Lieu : Rixensart Wallonia
Société : 1925 GlaxoSmithKline LLC
Détail de l'offre : change management,..or a related field.Significant pharmacovigilance experience relating to Safety Evaluation and Risk Management,..
Postuler |
Site source : Talent BE
Lieu : Rixensart Wallonia
Société : 1925 GlaxoSmithKline LLC
Détail de l'offre : Project Management,..Pharmacovigilance Scientists - Associate Director/ Director/ Senior Director Positions in GSK Safety Evaluation and Risk Management (SERM) - Specialty Safety Business.Exciting opportunities to make a significant impact on patie..
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Site source : Talent BE
Lieu : Wavre Wallonia
Société : 1925 GlaxoSmithKline LLC
Détail de l'offre : We provide pharmacovigilance and comprehensive benefit-risk management for advanced Respiratory medicines and devices,..
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Site source : Talent BE
Lieu : Rixensart Wallonia
Société : 1925 GlaxoSmithKline LLC
Détail de l'offre : Scientific/Medical Knowledge PV ExpertiseLeads Pharmacovigilance and Risk Management Planning and develops strategy for approach to evaluation of issues in the clinical matrix.Leads the safety component of global regulatory submissions. Expert evaluation skills and analytical think..
Postuler |
Site source : Talent BE
Lieu : Rixensart Wallonia
Société : 1925 GlaxoSmithKline LLC
Détail de l'offre : product incidents) and ensures that risk-reduction strategies are implemented appropriately.Facilitates safety governance/SRTs in the clinical development and post marketing settings by assisting in the establishment and operation of cross-functional teams in any SERM to detect and address..
Postuler |
Site source : Talent BE
Lieu : Rixensart Wallonia
Société : 1925 GlaxoSmithKline LLC
Détail de l'offre : Scientific/Medical Knowledge PV ExpertiseLeads Pharmacovigilance and Risk Management Planning and develops strategy for approach to evaluation of issues in the clinical matrix.Leads the safety component of global regulatory submissions. Expert evaluation skills and analytical think..
Postuler |
Site source : Talent BE
Lieu : Wavre Wallonia
Société : 1925 GlaxoSmithKline LLC
Détail de l'offre : product incidents) and ensures that risk-reduction strategies are implemented appropriately.Facilitates safety governance/SRTs in the clinical development and post marketing settings by assisting in the establishment and operation of cross-functional teams in any SERM to detect and address..
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Site source : Talent BE
Lieu : Brussels Brussels
Société : IQVIA
Détail de l'offre : and human ingenuity to drive healthcare forward.Associate Director/Director,..FSP solutions means that instead of outsource study by study we outsource function by function...
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Site source : Talent BE
Lieu : Zaventem Flanders
Société : IQVIA
Détail de l'offre : ranging from a simple staff augmentation requirement to a hybrid FSP model with staff oversight and transfer of processes. Responsibilities• Work with management to identify target customers,..
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Site source : Talent BE
Lieu : Zaventem Flanders
Société : IQVIA
Détail de l'offre : and execution of implemented plans for assigned region.RequirementsAt least 8 years’ experience as a BD Director in a CRO environmentUnderstanding of the clinical process (PH I – IV).Ideally extensive knowledge across Data Sciences,..
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Site source : Talent BE
Lieu : Brussels Brussels
Société : IQVIA
Détail de l'offre : clinical data management and medical writing for Research and development activities...ranging from a simple staff augmentation requirement to a hybrid FSP model with staff oversight and transfer of processes. Responsibilities• Work with management to identify target custo..
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