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International Scientific Director (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Projektbeschreibung
REFERENZNUMMER:
358866/11
IHRE AUFGABEN:
-Responsible for the development of the insights strategy as part of the overall medical strategy
-Responsible for external stakeholders mapping and maintains an oversight of stakeholder engagement, medical societies, collaborative groups, nurses and patient associations
-Responsible for advisory boards execution for the product(s)/disease area and contribution to the execution of evidence generation activities
-Staying abreast of internal and external developments, trends and other dynamics relevant for the assigned disease area to maintain a fully current view and perspectives of external influences
IHRE QUALIFIKATIONEN:
-PhD in life sciences (e.g. biologist, pharmacist), Pharm D, nurse, MD with no relevant clinical practice experience
-Experience with pre-clinical/clinical research required (academic research or in pharma industry)
-Good understanding of drug development process and related regulatory requirements and experience in implementation of clinical trials
-Expertise with a wide range of data/ information and knowledge about principles of data analysis and interpretation is required
-Fluency in written and spoken English
WEITERE QUALIFIKATIONEN:
Medical affairs manager
358866/11
IHRE AUFGABEN:
-Responsible for the development of the insights strategy as part of the overall medical strategy
-Responsible for external stakeholders mapping and maintains an oversight of stakeholder engagement, medical societies, collaborative groups, nurses and patient associations
-Responsible for advisory boards execution for the product(s)/disease area and contribution to the execution of evidence generation activities
-Staying abreast of internal and external developments, trends and other dynamics relevant for the assigned disease area to maintain a fully current view and perspectives of external influences
IHRE QUALIFIKATIONEN:
-PhD in life sciences (e.g. biologist, pharmacist), Pharm D, nurse, MD with no relevant clinical practice experience
-Experience with pre-clinical/clinical research required (academic research or in pharma industry)
-Good understanding of drug development process and related regulatory requirements and experience in implementation of clinical trials
-Expertise with a wide range of data/ information and knowledge about principles of data analysis and interpretation is required
-Fluency in written and spoken English
WEITERE QUALIFIKATIONEN:
Medical affairs manager
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges