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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
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Head of Biostatistics Department

Søborg

Do you have profound leadership experience and sound knowledge of clinical development?

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(Senior) Regulatory Professionals for CagriSema Obesity & Amylin

Søborg

Would you like to drive regulatory strategies within weight management for initial submissions to authorities on a global scale?

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Senior RA Professional for Development Project within Obesity

Søborg

Are you able to cut through complexity and drive regulatory strategies for high impact projects and would you like to work together with...

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Statistical Specialist

Søborg

Are you a highly experienced statistician looking for an opportunity to use your statistical knowledge and quality mindset to bring clinical projects to registration and market?

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Region Midtjylland

Data-analysts/Statisticians/Pharmacoepidemiologists at the Psychosis Research Unit of Aarhus University Hospital Psychiatry

Aarhus N

A 2-year full-time position as data-analyst/statistician/pharmacoepidemiologist is available at the...

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Senior Statistician

Søborg

Are you a highly experienced statistician looking for an opportunity to use your statistical knowledge and quality mindset to bring clinical projects to registration and market?

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