Regulatory Affairs: Succeed as consultant, Denmark
My client, a consultancy firm investing in the professional growth of young talents is currently looking for Pharma Regulatory Affairs Specialists based in Denmark and willing to kick-start a successful career as consultant : this is the occasion for you to develop a competitive and strong technical profile and maximize your income potential by collaborating with the main actors of the Danish pharmaceutical market with the job security granted by a permanent contract.
As a Regulatory Affairs Consultant, you will be hired on a permanent basis by my client who will allow you to add your value to different technical projects for different firms on long term missions and therefore enhance the technical skills which will help you out to specialize in the aeras you prefer.
Compared to a Regulatory Affair specialist working for only one pharmaceutical company, as regulatory affair consultant involved on different projects for different firms on a long term, you will develop a knowledge of process, procedures, methods and market trends which will make your profile more and more attractive and, consequently, your earning potential bigger and bigger year after year.
Main requirements to apply for this position
- 2 years experience in the regulatory affairs for the pharmaceutical field
- Commercial mind-set
- Danish native speaker
How to apply
Submit you most up to date Word format CV to Mariavittoria Ciniglio by WED 19.07.2017, sending an email to email@example.com : I will contact you to help you out in finding the job on the pharma market which better suits your expectations and tell you more about this opportunity.
Do you know someone who could be suitable for this role in Denmark? By recommending them to me, if they are hired by my client you will get a precious reward.
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