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Clinical Trial Manager (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Projektbeschreibung
REFERENZNUMMER:
244209/11
IHRE AUFGABEN:
-Provide direction and leadership to one or more clinical operations teams
-Contribute to the development and management of the study timelines, resources, budget, risk and quality plans
-Provide clinical operations expertise to ensure operational feasibility and delivery
-Oversee forecasting of clinical/non-clinical supplies
-Deliver the operational elements of the study plan
-Provide the day-to-day operational management of CROs and vendors to ensure delivery against contracted scope of work
-Identify areas of best practice and process improvements
-Ensure study adherence to ICH/GCP and SOPs
IHRE QUALIFIKATIONEN:
-Proven clinical development experience concerning the operational aspects of all stages of clinical studies preferably working in a global environment
-Profound experience in working with CROs, drug supply management and planning operational activities to achieve database lock
-Experience in project managing operational aspects of a clinical study including development of timelines, budgets and resource plans
-Good knowledge of ICH GCP
-Proven ability to successfully achieve results within a multi-cultural and geographically diverse team
-Experience in working as part of a large team and leading small study or functional teams
-Fluent English
WEITERE QUALIFIKATIONEN:
Clinical trial manager
244209/11
IHRE AUFGABEN:
-Provide direction and leadership to one or more clinical operations teams
-Contribute to the development and management of the study timelines, resources, budget, risk and quality plans
-Provide clinical operations expertise to ensure operational feasibility and delivery
-Oversee forecasting of clinical/non-clinical supplies
-Deliver the operational elements of the study plan
-Provide the day-to-day operational management of CROs and vendors to ensure delivery against contracted scope of work
-Identify areas of best practice and process improvements
-Ensure study adherence to ICH/GCP and SOPs
IHRE QUALIFIKATIONEN:
-Proven clinical development experience concerning the operational aspects of all stages of clinical studies preferably working in a global environment
-Profound experience in working with CROs, drug supply management and planning operational activities to achieve database lock
-Experience in project managing operational aspects of a clinical study including development of timelines, budgets and resource plans
-Good knowledge of ICH GCP
-Proven ability to successfully achieve results within a multi-cultural and geographically diverse team
-Experience in working as part of a large team and leading small study or functional teams
-Fluent English
WEITERE QUALIFIKATIONEN:
Clinical trial manager
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges