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Medical & Scientific Relations Manager (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Support
Projektbeschreibung
REFERENZNUMMER:
300560/11
IHRE AUFGABEN:
-Build and develop enduring peer-to-peer relationships with HCPs and institutions, creating constructive cross-functional partnerships with internal and external stakeholders to meet the customer's medical needs across the medicines' lifecycle
-In response to an unsolicited request for information, communication of scientific data on the VAC portfolio, including off-label indications and on compounds in development where specifically requested
-Support the management of local/national Advisory Boards (speaker briefings for symposia and congresses etc.)
-Provide high-quality, accurate, balanced and directed information to key customers and stakeholders in response to unsolicited requests for information
-Ensure customer intelligence and customer findings are fed back into the organisation to generate customer insights and leverage medical opportunities
-Support disease area medical strategies by providing support for the implementation of local non-interventional studies and follow up on IIR opportunities
-Support feasibilities for phase 1-4 studies, support in the management of local advisory boards and interact with local clinical investigators and other key medical and scientific activities
-Report to Medical Advisor, MSR Team Leader, Medical Team Leader, Medical Director or other senior medical functions
IHRE QUALIFIKATIONEN:
-Medical, pharmacy or science degree, preferably on postgraduate level
-Fluency in German and/or French and business fluency in English
-In-depth knowledge of the therapy area, immunology/vaccines, the relevant medicines in the portfolio and the pipeline
-Understanding of the compliance framework for medical interactions in relation to local regulations
-Good understanding of clinical research and the ability to critically evaluate clinical study protocols, reports and publications
-Strong presentation and networking skills
-High degree of cross-functional collaboration
-Ability to clearly communicate information and concepts which may be complex in nature
-Good understanding of the local (Swiss) health care environment at national, regional and local level
-Good knowledge of pharmacovigilance and regulatory legislation and how it impacts the product portfolio
-Good knowledge of drug development
-Knowledge of health economics and their impact on medical decision making
WEITERE QUALIFIKATIONEN:
Medical affairs manager
300560/11
IHRE AUFGABEN:
-Build and develop enduring peer-to-peer relationships with HCPs and institutions, creating constructive cross-functional partnerships with internal and external stakeholders to meet the customer's medical needs across the medicines' lifecycle
-In response to an unsolicited request for information, communication of scientific data on the VAC portfolio, including off-label indications and on compounds in development where specifically requested
-Support the management of local/national Advisory Boards (speaker briefings for symposia and congresses etc.)
-Provide high-quality, accurate, balanced and directed information to key customers and stakeholders in response to unsolicited requests for information
-Ensure customer intelligence and customer findings are fed back into the organisation to generate customer insights and leverage medical opportunities
-Support disease area medical strategies by providing support for the implementation of local non-interventional studies and follow up on IIR opportunities
-Support feasibilities for phase 1-4 studies, support in the management of local advisory boards and interact with local clinical investigators and other key medical and scientific activities
-Report to Medical Advisor, MSR Team Leader, Medical Team Leader, Medical Director or other senior medical functions
IHRE QUALIFIKATIONEN:
-Medical, pharmacy or science degree, preferably on postgraduate level
-Fluency in German and/or French and business fluency in English
-In-depth knowledge of the therapy area, immunology/vaccines, the relevant medicines in the portfolio and the pipeline
-Understanding of the compliance framework for medical interactions in relation to local regulations
-Good understanding of clinical research and the ability to critically evaluate clinical study protocols, reports and publications
-Strong presentation and networking skills
-High degree of cross-functional collaboration
-Ability to clearly communicate information and concepts which may be complex in nature
-Good understanding of the local (Swiss) health care environment at national, regional and local level
-Good knowledge of pharmacovigilance and regulatory legislation and how it impacts the product portfolio
-Good knowledge of drug development
-Knowledge of health economics and their impact on medical decision making
WEITERE QUALIFIKATIONEN:
Medical affairs manager
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges