Clinical Supply Program Manager – Lille Cedex, Belgium

Clinical Supply Program Manager
Start date: ASAP
Duration: 12 months
For one of our partners in the region of Braine l’Alleud, we are currently looking for a Clinical Supply Program Manager. You have the CTS accountability at program level. You actively drive trial and packaging design and supply chain optimization, and ensuring full visibility of CTS on clinical development plans and compound information. You’ll be a program matrix leader within CTS, overseeing trial supply execution and driving risk and budget management through other functions.
Your responsibilities:

  • Define and consolidate a supply strategy to ensure adequate and sufficient forecasting of drug product for assigned programs
  • Create and maintain high level supply plan for all upcoming trials as soon as created in EPPM (Enterprise Project and Portfolio Management system), until Clinical Supply Manager assignment
  • Compile the forecasted trial budgets into a compound budget and provide regular updates through the company budget exercises
  • CTS interface for the Technical Lead and Clinical Program Director and Lead Clinical Development Representative, fostering a close partnership
  • Represent CTS in CST (Clinical Satellite Team) meetings and ensure CTS requirements and expectations are met
  • Represent CTS in TST (Technical Satellite Team) and address requirements for CMC related activities (development of formulation, stability program, shelf life extension)
  • Ensure availability of compound information and knowledge in CTS (formulation types, manufacturing sites, shelf life, clinical and technical challenges)
  • Lead and maintain structured oversight on clinical trials (forecasted and on-going) per compound to ensure no supply chain disruption and adequate budget, providing guidance and support to other CTS functions, Global Distribution, Logistics and QA
  • Drive and champion department transformation, lead and contribute to projects

Your profile:

  • Master degree in sciences
  • Minimum 5 years of CTS relevant experience (in pharmaceutical manufacturing or packaging, clinical trials and, or supply chain)
  • Clinical supply experience is mandatory
  • Experience with Project and Supply Chain Management
  • Experience with and knowledge of cross-functional root cause, impact analysis and action plan
  • Knowledge of GxPs
  • Creative, problem-solving and strategic thinking team player who’s result driven and has strong financial, influencing, negotiation and leadership skills
  • Ability to travel domestically or internationally for business reasons on an as needed basis
  • Fluent communication and presentation skills in English

Our offer:

  • A position with responsibility within a leading international company
  • Personal development through learning on the job and additional external trainings
  • A market oriented compensation, including a range of fringe benefits

Powered by WPeMatico