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Expert Clinical Manager (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Support
Projektbeschreibung
REFERENZNUMMER:
303723/11
IHRE AUFGABEN:
-Conduct operational aspects of global oncology clinical trial(s) under the management of the Clinical Trial Head (CTH) and also manage tasks independently
-Ensure all operational trial deliverables are met according to timelines, budget, operational procedures, quality/compliance and performance standards
-Management of clinical study material
-Prepare clinical outsourcing specifications
-Responsible for management of Contract Research Organizations (CROs)
-Support the development, management and tracking of trial budget
-Responsible for accuracy of trial information in all trial databases and tracking systems
-Responsible for the ongoing scientific review and validation of clinical data (member of the Data Review Team)
-Responsible for education, implementation and compliance to standards (SOPs) and best practice
IHRE QUALIFIKATIONEN:
-Profound experience in clinical trial management
-Working experience in oncology field highly desirable
-Experience und budget tracking, management and development
-Experience within CRO management
-Working experience with trial databases and tracking systems
-Strong personal and communication skills
-Fluency in English
WEITERE QUALIFIKATIONEN:
Clinical project manager, Clinical trial assistant
303723/11
IHRE AUFGABEN:
-Conduct operational aspects of global oncology clinical trial(s) under the management of the Clinical Trial Head (CTH) and also manage tasks independently
-Ensure all operational trial deliverables are met according to timelines, budget, operational procedures, quality/compliance and performance standards
-Management of clinical study material
-Prepare clinical outsourcing specifications
-Responsible for management of Contract Research Organizations (CROs)
-Support the development, management and tracking of trial budget
-Responsible for accuracy of trial information in all trial databases and tracking systems
-Responsible for the ongoing scientific review and validation of clinical data (member of the Data Review Team)
-Responsible for education, implementation and compliance to standards (SOPs) and best practice
IHRE QUALIFIKATIONEN:
-Profound experience in clinical trial management
-Working experience in oncology field highly desirable
-Experience und budget tracking, management and development
-Experience within CRO management
-Working experience with trial databases and tracking systems
-Strong personal and communication skills
-Fluency in English
WEITERE QUALIFIKATIONEN:
Clinical project manager, Clinical trial assistant
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Sonstiges