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LEO Pharma, Ballerup
If you are interested in early stage drug development and skin disease this job could be a great opportunity for you.
Your overall objective is to contribute to the development of new drugs and treatments for people with skin diseases. You will support the organisation with medical input shaping early stage development of our project pipeline and explorative trials establishing new indications. You will unfold your skills in various project teams in a role as their Medical Expert. Your primary tasks will be to:
- Act as medical lead for Translational Medicine for disease indication development programmes
- Support clinical trials in early clinical development (Clinical Proof of Concept plans and clinical trials ranging from First in Human to Proof of Concept phase 2a trials)
- Analyse, interpret and report on data from clinical trials and literature
Novo Nordisk A/S, Bagsværd
Is drug safety important to you? Are you excited by digging into information to find answers? Do you want to play a key role in ensuring highest safety and lowest possible risk to patients that use Novo Nordisk products? You may be our new colleague in Safety Surveillance GLP1 Diabetes.
You will be responsible for the ongoing safety surveillance of one or more products used in the treatment of Type 2 Diabetes. This responsibility includes critical analysis and medical evaluation of the emerging safety data, establishment of the product safety profile during development and maintenance of the labelling for marketed products, and communication about the benefit-risk assessment. Once the analysis is done, you will be required to present the data to a group of highly experienced physicians, scientist and managers within the company.
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