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Zealand Pharma A/S

Regulatory Affairs Clinical Specialist

Søborg

Due to many activities in our exciting clinical development projects, we are seeking two new colleagues to our Regulatory Affairs function.

Your key responsibilities will be to contribute with regulatory expertise to global strategies and execution within your assigned project(s). You will be the regulatory responsible in the clinical trial teams and provide regulatory guidance and support for the planning, execution, and reporting of clinical trials worldwide.

Zealand Pharma A/S

Regulatory Affairs Professional

Søborg

If you are passionate about drug development within Diabetes and Obesity and want to be a subject matter expert in a leading international...

Senior Scientist

Måløv

Would you like to be a part of a growing business area within Novo Nordisk and enjoy working in a dynamic environment involving teamwork and cross-functional cooperation?

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