Clinical Trial Supply Professional

Would you like to play a key role in the development of our growing portfolio together with a 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 our efforts. 

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

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

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.

Quality Mindset

You hold an MSc or a BSc degree within Pharmacy, Biology or equivalent. You have 3-5 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 adjust 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 sponsored clinical trials from phase I-IV. In Clinical Trial Supplies you will ghave 5 colleagues, who are dedicated to their role in our clinical trials.

Further information and application deadline

In case you have any further questions, please contact Manager Jørgen Rigtrup at +45 3177 4791.

Deadline for submitting your application is June 10th 2018.

We look forward to receiving your application.

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About LEO Pharma
LEO Pharma helps people achieve healthy skin. By offering care solutions to patients in more than 100 countries globally, LEO Pharma supports people in managing their skin conditions.
Founded in 1908 and owned by the LEO Foundation, the healthcare company has devoted decades of research and development to delivering products and solutions to people with skin conditions.
LEO Pharma is headquartered in Denmark and employs around 5,300 people worldwide.
For more information, visit
Application deadline: 10/06/2018

Location: Ballerup, Greater Copenhagen, DK

Job type: Permanent

Working hours: Full-time

Contacts: Jørgen Rigtrup
Mobile: +4531774791