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Senior Clinical Trial Supply Management Professional

1 miesiąc temu


Gdańsk, Pomerania, Polska LEO Pharma Pełny etat

Key Responsibilities:

As a Senior Clinical Trial Supply Management Professional, you will be responsible for independently planning and coordinating clinical supply activities for all development phases, both in-house and outsourced trials. You will maintain compliance with regulatory guidelines and ensure collaboration between various departments and external vendors.

Requirements:

  • Reviewing overall clinical trial protocols and related documents.
  • Developing efficient packaging designs and visit schedules.
  • Building and maintaining accurate clinical supply demands aligned with protocol requirements and key study parameters.
  • Implementing optimal resupply strategies with proactive planning and appropriate lead-time.
  • Proficiency in setting up and maintaining Interactive Response Technology (IRT) Systems.
  • Consolidating and supervising clinical trial budgets in collaboration with key stakeholders.
  • Collaborating effectively across various organizational levels, functions, and geographies to achieve goals and objectives.

What We Offer:

LEO Pharma is a global leader in medical dermatology, dedicated to leaving a lasting impact. Our innovative approach sets us apart, and we value diversity and welcome applications from all qualified candidates. Join our passionate team and be yourself as we work together to make a difference.