172 offres d'emploi Associate Director, Study Management - |
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Lieu : Zaventem Flanders
Société : IQVIA
and speaking at trade shows and industry conferences.• Identify and provide strategic information to support Business Development’s annual plans.• Provide support and refine pricing algorithms to facilitate and standardize proposal budgeting process.• Establish and manage an effect..
Postuler |
Lieu : Brussels Brussels
Société : IQVIA
and human ingenuity to drive healthcare forward.Associate Director/Director,..clinical data management and medical writing for Research and development activities...
Postuler |
Lieu : Brussels Brussels
Société : IQVIA
clinical data management and medical writing for Research and development activities...and human ingenuity to drive healthcare forward.Associate Director/Director,..
Postuler |
Lieu : Zaventem Flanders
Société : IQVIA
and speaking at trade shows and industry conferences.• Identify and provide strategic information to support Business Development’s annual plans.• Provide support and refine pricing algorithms to facilitate and standardize proposal budgeting process.• Establish and manage an effect..
Postuler |
Lieu : Brussels Brussels
Société : IQVIA
FSP solutions means that instead of outsource study by study we outsource function by function...ranging from a simple staff augmentation requirement to a hybrid FSP model with staff oversight and transfer of processes. Responsibilities• Work with management to iden..
Postuler |
Lieu : Zaventem Flanders
Société : IQVIA
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,..
Postuler |
Lieu : Brussels Brussels
Société : IQVIA
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,..
Postuler |
Lieu : Zaventem Flanders
Société : IQVIA
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,..
Postuler |
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Lieu : Brussels Brussels
Société : IQVIA
and speaking at trade shows and industry conferences.• Identify and provide strategic information to support Business Development’s annual plans.• Provide support and refine pricing algorithms to facilitate and standardize proposal budgeting process.• Establish and manage an effect..
Postuler |
Lieu : Zaventem Flanders
Société : IQVIA
....FSP solutions means that instead of outsource study by study we outsource function by function...and execution of implemented plans for assigned region.RequirementsAt least 8 years’ experience as a BD Director in a CRO environmentUnderstanding of the clinical pro..
Postuler |
Lieu : Brussels Brussels
Société : IQVIA
and human ingenuity to drive healthcare forward.Associate Director/Director,..clinical data management and medical writing for Research and development activities...
Postuler |
Lieu : Zaventem Flanders
Société : IQVIA
and human ingenuity to drive healthcare forward.Associate Director/Director,..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 ..
Postuler |
Lieu : Wavre Wallonia
Société : 9627 Corixa Corporation
..Training in the principles of epidemiologic study design,..risk management plan,..public health,..Make presentations to the scientific,..
Postuler | Plus d'offres Associate Director, Epidemiology (Vaccines)
Plus d'offres - Wavre |
Lieu : Wavre Wallonia
Société : 9627 Corixa Corporation
Training in the principles of epidemiologic study design,....risk management plan,..compilation and interpretation and scientific writing for publication,..
Postuler | Plus d'offres Associate Director, Epidemiology (Vaccines)
Plus d'offres - Wavre |
Lieu : Wavre Wallonia
Société : 9627 Corixa Corporation
as well as literature reviews and compilation of existing epidemiologic data;Primary responsibility for development of study design and data collection for epi studies.Author final report summarizing study results...
Postuler | Plus d'offres Associate Director, Epidemiology (Vaccines)
Plus d'offres - Wavre |
Lieu : Wavre Wallonia
Société : 9627 Corixa Corporation
as well as literature reviews and compilation of existing epidemiologic data;Primary responsibility for development of study design and data collection for epi studies.Author final report summarizing study results...
Postuler | Plus d'offres Associate Director, Epidemiology (Vaccines)
Plus d'offres - Wavre |
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
Familiar with and considers overall business objectives and company strategy.Acts as a senior advisor and mentor within the team and beyond and serves as best practice resource within own discipline or as technical expert on cross functional teams or projects.Ensure all study man..
Postuler |
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
PMP) desirable.Proven experience in all aspects of clinical study planning and startup (including budget and resource planning) and in executing the complete range of clinical study activities,..
Postuler |
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
from startup through final study report.Experience in multiple Therapeutic Areas (oncology and immunology preferred)Requires substantial to extensive professional experience in relevant disciplines and substantial project management experience...
Postuler |
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
PMP) desirable.Proven experience in all aspects of clinical study planning and startup (including budget and resource planning) and in executing the complete range of clinical study activities,..
Postuler |
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
able to predict the result of action in advance and evaluate options to achieve goals. Who you areAt least 10-12 years in clinical research in a CRO or Pharmaceutical/Biotechnology Industry environment with at least 7 years of in-depth knowledge and experience in clinical trial managem..
Postuler |
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
audit & inspection leadership- interviewee & responses.Contribute to non-study -related initiatives in addition to study assignments...
Postuler |
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
PMP) desirable.Proven experience in all aspects of clinical study planning and startup (including budget and resource planning) and in executing the complete range of clinical study activities,..
Postuler |
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
from startup through final study report.Experience in multiple Therapeutic Areas (oncology and immunology preferred)Requires substantial to extensive professional experience in relevant disciplines and substantial project management experience...
Postuler |
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
Familiar with and considers overall business objectives and company strategy.Acts as a senior advisor and mentor within the team and beyond and serves as best practice resource within own discipline or as technical expert on cross functional teams or projects.Ensure all study man..
Postuler |
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