Senior Professional – Clinical Trial Supplies

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Ballerup

Do you want to unfold your skills from start to closure in global studies?

If you have some years’ experience within clinical trials, and you are ready for more and wider responsibility, we have just the right job waiting for you. At LEO Pharma we have set the very ambitious goal to become the world’s preferred dermatology care partner. To make this vision come true we invest massively in R&D and we have a highly promising pipeline, meaning we have a historically high number of studies in motion with more to come.

That is why we need you to unfold all of your good knowledge and positive personality across clinical trials from phase I-IV – in a very well functioning and harmonic team of experienced specialists.

Management of IMP outsourced related activities across phase I-IV

Your job is to ensure supplies to LEO Pharma’s global studies. More specifically, you will manage IMP outsourced related activities in connection with the conduct of Clinical Trials Phase I-IV. You will be involved in studies from start up to final round up which will provide you with challenges and learning opportunities far beyond the average – naturally with the best possible support from your very experienced colleagues. Your primary tasks will be to:

  • Handle quality related tasks – like deviations and other GMP related tasks
  • Participate/lead in cross-functional optimizing projects – e.g. reduction of lead time in studies
  • Create SOP´s and keep them updated
  • Present at Investigator/CRA meetings
  • Provide input to the Clinical Trial Protocol


  • You can look forward to a job with a high level of constructive interaction with external partners in CMOs and colleagues in e.g. R&D and trial management.

    3+ years’ experience within clinical trials and quality mindset

    We are looking for at profile with a high-level quality mindset and the structured way of working and overview it takes to never compromise on quality – including the ability to deliver within agreed deadlines. As a senior you must be able to move things forward on your own and know when it is time to ask for help. Additionally, you must like to create results as part of a team that prioritises collaboration and knowledge sharing. As part of this, we hope you bring a curious mind and a drive for shaping the future via positive sharing of ideas. Additionally, your CV comprises:

  • A university degree within pharma, biology or…
  • Min. 3 years of experience from working with clinical trials
  • A good understanding of IRT systems
  • A good overall GMP understanding


  • Clinical Trial Supplies – your new team

    Your will join a team of experienced and very dedicated clinical trial specialists. We are 7 in Ballerup where you will be based, and we have two colleagues in the US and one in Taiwan. We are part of Global Clinical Operations that is responsible for all LEO Pharma sponsored clinical trials from phase I-IV. Our working environment is friendly and welcoming and characterised by a helpfulness and team spirit. We believe that trust and respect are the foundation for the greatest results – first you need to feel appreciated and comfortable, then the results will follow.


    Information og data

    Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

    Arbejdsstedet er beliggende i Ballerup.

    Jobbet er oprettet på vores service den 20.12.2019, men kan have været deaktiveret og genaktiveret igen.

    Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
    • Øvrige
    • Ballerup
    • Onsdag den 15. januar 2020

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