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Description
The Director will lead medical/scientific and operational expertise into the planning and execution of the medical support activities of Celgene compounds for Dermatology for the EU.
Responsibilities:
Provides expert opinion on the current trends in the pathophysiology, diagnosis, existing and emerging treatment options as well as unmet medical needs in the therapeutic area to inform key medical and business decisions.
Build mutually valuable partnerships within the medical community through the execution of the EU Medical Affairs program.
Develop strong relationships with EU key opinion leaders, key professional societies and organizations in collaboration with global medical affairs and clinical colleagues through scientific dialogue pertinent to Celgene I&I interest.
Participate in and support EU clinical strategies in conjunction with EU commercial counterparts. Provide ongoing and interactive technical and medical expertise to execute on these strategies.
Provide expertise into the phase 3b/4 development for the EU.
Participate in and support EU Publication Plan.
Participate in formal scientific review of submitted EU Investigator Initiated Trials and related medical affairs activities (e.g. registry/database projects, epidemiological surveys etc.). Provide timely and interactive feedback to ensure adequate study progress.
Provide medical support to the EU medical affairs organizations including developing and delivering training curriculum and content.
Participate in EU advisory meetings with opinion leaders.
Actively participate on EU promotional review committees to ensure content is medically appropriate and compliant with internal and external requirements.
Experience/Qualifications:
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