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Archiviertes Projekt - Global Medical Director / Global Scientific Director (m/f/d)

Firmenname für PREMIUM-Mitglieder sichtbar

Juli 2020

nicht angegeben

CH-Basel

auf Anfrage

16.07.2020

490918/1-en

Projektbeschreibung

Ihre Aufgaben:
• Evidence Generation Strategy Planning and Execution
• Accountable for evidence generation activities for the assigned product (s) / Indication(s), including risk benefit assessment and medical monitoring in all medical affairs interventional studies
• Takes the role of Lead Scientific Responsible and acts as a member of the Study Management Team (SMT)
• Conduct review and approval of investigator initiated studies (IIS) and supported study proposals (incl. Review of affiliate study synopses and sign off of affiliate studies)
• As appropriate, provides medical expertise and scientific data to support Regulatory, Drug Safety, Health Economics and Public Policy strategy and documents
• As appropriate, represents PDMA and provides medical expertise to the appropriate Global Access teams and other relevant teams
• For some projects, the GMD may drive and lead the strategy of the integrated evidence generation activities, incl. Roche sponsored clinical studies, Investigator Initiated Studies (IIS), RWD
• Develop, advances and maintains TAE interactions and collaborations, incl. those aimed to set up and conduct evidence generation activities
• Represents Roche in peer-to-peer interactions with external collaboration partners, including in patient-company interactions. 
• Responsible for acting in line with legal, regulatory and company standards and codes of Practice
• Complete all required training modules as priority

Ihre Qualifikationen:
• Profound experience in pharma (either in Medical Affairs or Clinical Operations) 
• Experience in clinical study set up and management on a global level 
• Scientific education minimum Master or PhD
• Experience in Oncology / GI Cancer (GI Cancer is a plus but not at all necessary) 
• Experience with China as part of a global clinical study 
• Clinical Research additional trainings 
• Experience of partnership with therapeutic area experts and external organizations is strongly preferred 
• Previous experience with launch of drugs/indications is preferred

Ihre Vorteile:
• Dynamic and innovative market environment
• Flat hierarchies
• Good infrastructure
• High proven employee satisfaction based on annual surveys

Projektdauer: 12 MM++


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