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Contribute with regulatory expertise to global strategies and tactics
Develop regulatory documentation for submission to Health Authorities globally, e.g. clinical trial applications, briefing packages, paediatric plans, and responses to health authority questions
Represent Regulatory Affairs in global clinical trial teams and other cross-functional teams
Collaborate effectively with cross-functional stakeholders such as project managers, medical and non-medical specialists, statisticians, and medical writers

Regulatory Affairs Professional, RA Diabetes, CV, Liver and Rare Disease
Søborg, Capital Region of DenmarkDKK570K - DKK838K / yearPosted 1 weeks ago
Full-timeonsitemid