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    For a business partner from the pharmaceutical sector, we are currently looking for a skilled professional to manage Clinical Supply Systems. A secure and fair salary and good social benefits are just as important to you as a responsible job and a long-term perspective? Then join us - your satisfaction is our goal Apply directly online now We value equal...

Clinical Supply Project Coordinator

vor 2 Monaten


Ludwigshafen am Rhein, Rheinland-Pfalz, Deutschland GULP – experts united Vollzeit

Begin your journey as a Project Manager with us at GULP – experts united . We are currently seeking a Clinical Supply Project Associate to support our esteemed partner in the pharmaceutical sector . This role offers an exciting opportunity to engage in meaningful work within a collaborative environment.

What We Provide

  • Competitive salary with job stability through our corporate affiliation
  • Comprehensive social benefits, including holiday and vacation bonuses
  • Travel expense reimbursement
  • Up to 30 days of annual leave
  • Opportunities for professional development through e-learning
  • Monthly employee perks, covering various sectors such as technology and fashion

Key Responsibilities

  • Assist Clinical Supplies Project Managers (CSPM) in managing clinical trial materials
  • Serve as a primary contact for standardized processes across multiple global clinical trials
  • Aid in the planning, organization, and coordination of clinical trial materials
  • Ensure timely provision of clinical trial materials by managing orders for packaging and labeling
  • Support project managers in extending the availability of clinical trial materials
  • Assist with revisions of clinical trial materials as required
  • Communicate with relevant stakeholders regarding any uncertainties or timeline adjustments
  • Collaborate on the development of innovative strategies for clinical trial material provision
  • Participate in local project teams
  • Present concepts in both local and global project forums
  • Contribute to the creation and revision of GMP and GCP-related standard operating procedures (SOPs)

Your Qualifications

  • Completed scientific or medical education (Bachelor's degree or equivalent)
  • Foundational knowledge of project management principles
  • Experience in development or within GMP/GCP environments
  • Familiarity with GMP/GCP regulations
  • Strong IT proficiency
  • Excellent command of both German and English
  • Ability to work in a structured manner and independently manage daily tasks
  • Goal-oriented and self-motivated work ethic
  • Strong teamwork and communication skills