The product information (label) is the outcome and conclusion of the entire clinical development. Do you understand the needs of health authorities, health care professionals, payers and patients - and can you realise this knowledge to optimise the label?
You will be responsible for driving the global labelling strategy for one or several of our products.
Your primary tasks will be to:
You have a Master’s degree or bachelor within science e.g. pharmaceutics, biomedicine, chemical engineer or a related field, and experience within the regulatory or clinical development area (>5years).
The ideal candidate is curious, proactive, and eager to learn. Collaborative team-players with strong project management and communication skills are highly valued.
You will be part of a department of dedicated labelling specialists. Our vision is to be strong strategic partners throughout the life-cycle of our products. We are on a journey and you will be part of a department where we learn together.
If you have any questions, please do not hesitate to contact Merete Peder-sen, Head of Labelling Strategy (+45 22700866), Global Regulatory Affairs.
Please apply via the link at our website and remember to attach application and CV.
At LEO Pharma, we seek passionate, entrepreneurial and solutions-oriented colleagues, and consistently ensure that our people can proactive-ly develop their capabilities and fulfil their potential. Together, we can em-brace the changing healthcare landscape and grasp strategic business op-portunities. The result: life-enhancing products that bring hope to patients living with chronic dermatologic diseases. With a robust R&D pipeline we have a strong vision to become the preferred dermatology care partner.