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Associate Director - International Advertising and Promotion (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Marketing, Support
Projektbeschreibung
REFERENZNUMMER:
299116/11
IHRE AUFGABEN:
-Accountable for the client's Commercial Medical Legal Regulatory (CMLR) process which defines the review of promotional and non-promotional materials for selected products
-Responsible and accountable for reviewing and assessing internationally produced promotional and non-promotional items for the Gastrointestinal and Internal Medicine Business Units with specific product responsibilities
-Provide expert regulatory review of the internationally developed promotional materials for assigned products within the Gastrointestinal and Internal Medicine Business Unit
-Conduct detailed review and evaluation of adequacy of clinical evidence provided to support proposed claims, assess consistency of proposed claims with EMEA approved prescribing information
-Attend the pre-CMLR concept meetings to provide expert guidance
-Assist marketing in the planning and prioritization of the review of promotional and non-promotional materials according to International CMLR Standards (ICS) in close collaboration with Medical and Legal
IHRE QUALIFIKATIONEN:
-B.A. or B.S. degree or higher
-Profound experience in pharmaceutical/biologics regulatory, legal, scientific, medical, or marketing disciplines
-Experience in International CMLR review and approval process of pharmaceutical/biologics promotion
-Ability to understand EFPIA and international (ex-US) regulations basics regarding advertising and promotion for prescription products
-Ability to understand the basics in pharmaceutical promotion development and review process
-Excellent English communication skills, in both written and verbal form
WEITERE QUALIFIKATIONEN:
Marketing manager
299116/11
IHRE AUFGABEN:
-Accountable for the client's Commercial Medical Legal Regulatory (CMLR) process which defines the review of promotional and non-promotional materials for selected products
-Responsible and accountable for reviewing and assessing internationally produced promotional and non-promotional items for the Gastrointestinal and Internal Medicine Business Units with specific product responsibilities
-Provide expert regulatory review of the internationally developed promotional materials for assigned products within the Gastrointestinal and Internal Medicine Business Unit
-Conduct detailed review and evaluation of adequacy of clinical evidence provided to support proposed claims, assess consistency of proposed claims with EMEA approved prescribing information
-Attend the pre-CMLR concept meetings to provide expert guidance
-Assist marketing in the planning and prioritization of the review of promotional and non-promotional materials according to International CMLR Standards (ICS) in close collaboration with Medical and Legal
IHRE QUALIFIKATIONEN:
-B.A. or B.S. degree or higher
-Profound experience in pharmaceutical/biologics regulatory, legal, scientific, medical, or marketing disciplines
-Experience in International CMLR review and approval process of pharmaceutical/biologics promotion
-Ability to understand EFPIA and international (ex-US) regulations basics regarding advertising and promotion for prescription products
-Ability to understand the basics in pharmaceutical promotion development and review process
-Excellent English communication skills, in both written and verbal form
WEITERE QUALIFIKATIONEN:
Marketing manager
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Marketing/Vertrieb, Sonstiges