Denmark Job Openings
Novo Nordisk
Safety Surveillance Specialist
Søborg
September 11, 2024
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Chairing cross-functional drug safety committees
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Preparing communication about the benefit risk assessment
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Contributing to development of clinical study designs and protocols
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Communicating with external parties related to clinical safety monitoring such as Data Monitoring Committees
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Representing Safety Surveillance in cross-functional teams
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A master’s degree within Medicine or Natural Sciences e.g., Doctor of Medicine (MD), Doctor of Veterinary Medicine (DVM), Master of Science in Pharmacy or in human biology/physiology or equivalent, eventually complemented by a Ph D/research experience
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Several years of experience within Safety Surveillance and development in the pharmaceutical industry
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Interest/experience in data analysis and analysis tools (e.g. JMP and/or Qlik Sense)
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Experience with rare diseases, hemophilia or hemoglobinopathies is an advantage
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The ability to work independently as well as to collaborate in a continuous developing environment
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