LEO Pharma

Clinical Trial Supply Senior Professional

Would you like to play a key role in the development of our growing portfolio together with a Global, friendly, ambitious and professional team of Clinical Trial Supply Professionals? 

LEO Pharma is committed to improving the lives of people with skin diseases around the world. With our ambitious aspiration to help more than 125 million people by 2025, LEO Pharma is looking at new and innovative solutions - now also having entered into development of biologic treatments. LEO Pharma is set to become the world dermatology leader – offering the most diverse range of treatment solutions to meet the individual needs of people with skin diseases. 

IMP for Clinical Trials

If your experience and expertise covers handling of Investigational Medicinal Products for Clinical Trials and you are a well-structured, detail orientated and systematic team player, you might be the one that we are looking for to strengthen LEO Pharma A/S  

As a Clinical Trial Supply Sr. Professional you will join a very dedicated team, who is responsible for managing IMP outsourced related activities in connection with the conduct of Clinical Trials Phase I-IV. You will be working according to given LEO Pharma procedures and relevant GMP, GCP, GDP and regulatory requirements. You will also:

  • Create SOP´s and keep them updated.
  • Participate/lead in cross-functional optimizing projects
  • Present at Investigator/CRA meetings
  • Need to hold a strong understanding for IRT systems
  • Provide input to the Clinical Trial Protocol

Working in Clinical Trial Supply will also demand a high level of interaction with both internal and external Stakeholders e.g. R&D Quality, Contract Manufacturing Organisations (CMO), Clinical Trial Managers (CPMs) and departments across LEO Pharma A/S.


Quality Mindset

You hold a MSc. or BSc. Degree within Pharmacy, Biology or equivalent. You have years of experience within the Pharmaceutical industry and the area of Clinical Trials. You never compromise with quality, and have the ability to plan ahead. You strive to meet any given deadline, and always keep focus on the end result being of the highest quality.

On a personal level you are open minded, easily adjusted to changes and thrive in a fast paced work environment.


Global Clinical Operations – your new work place

Global Clinical Operations in Ballerup is responsible for all LEO Pharma A/S sponsored clinical trials from phase I-IV. In Clinical Trial Supplies you will gain 8 colleagues, who are dedicated to their role in our clinical trials.  If you have any questions to the position please contact Manager Joergen Rigtrup, GEUDK@leo-pharma.com. 


We look forward to receiving your application.


Application deadline 28 January 2019 



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Ballerup, Greater Copenhagen


Jørgen Rigtrup

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