Clinical Trial Supply Manager (m/f/d)

Our client’s mission is to make exceptional, innovative biopharmaceuticals to improve the lives of patients suffering from serious diseases. Innovative technologies and smart development strategies are central to our approach. Success is created by our people, who focus on excellence in all they do, collaborate closely across disciplines. Our client is driven by a desire to make the medicines of tomorrow a reality. Guided by mutual respect and trust, each member of the team is given the opportunity to develop and flourish within this exciting and inspiring environment.

 

We are searching for a

Clinical Trial Supply Manager (m/f/d)

  • Bereich:

    Medical

  • Berufssparte:

    Forschung/Entwicklung

  • Arbeitsregion:

    Near Munich

  • Art der Anstellung:

    Permanent

  • Kennziffer:

    26242

  • Aktualisierung:

    15.10.2020

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Your tasks

  • Development of appropriate packaging and supply strategies for clinical trial supplies, e. g. labeling requirements, packaging layout, depot structure and distribution setup for global clinical trials, together with the relevant multiple internal interfaces
  • Management of external vendors for IMP labeling packaging, storage, comparator sourcing and logistics
  • Contribution to vendor selection processes, vendor and contract management as well as budget monitoring processes
  • Input to IRT requirement specifications and performance user acceptance testing
  • Management and tracking of IMP inventories, takeover of supply roles in IRT systems
  • Contribution to supply planning and forecasting procedures for clinical programs, monitoring and maintenance of supply forecasts
  • Representation of Clinical Trial Supply in the multidisciplinary clinical trial team

Your qualifications

  • Degree in Life Sciences, Pharmacy, Chemical Engineering or Bioengineering
  • Several years of experience in clinical supply management
  • Proven track record in biotech or pharmaceutical industry
  • Expertise in GxP requirements for Clinical Trial Supply Management
  • Clear commitment to work in the highly regulated area of pharmaceutical development
  • Highly motivated and open-minded team player with well-developed interpersonal abilities
  • Excellent communication skills, both in English and German
  • Sound knowledge of Microsoft Office applications 

What we offer

  • Creative working in X-functional teams
  • Open and appreciative corporate culture
  • Multicultural environment 
  • Working in an attractive, high-quality equipped building with restaurant
  • Free sports and language courses

Ihre Ansprechpartnerin

Bettina Cöppicus
Senior Personalberaterin

Anschrift

Optares ICM GmbH & Co. KG
Bettina Cöppicus
Heiligengeist Höfe 8
26121 Oldenburg