Clinical Supply Set-up Manager

Clinical Supply Set-up Manager

CROMSOURCE

Braine l'Alleud, Belgium

The Clinical Supply Set-Up Manager is accountable for the project management of the set-up of study supply and new capabilities at Clinical Trial Supplies (CTS) Department.

He/she plans, coordinates and communicates clinical supply activities for all applicable clinical trials during their set-up phase, aiming to achieve optimal quality, time and budget.

He/she implements the strategy defined in collaboration with stakeholders and provides visibility on clinical supply chain during trial set-up.

Responsibilities:

  • Gathers and challenges clinical and supply assumptions to trigger the study supply optimization
  • Defines an Investigational Medical Product (IMP) supply strategy to ensure adequate and sufficient forecasting of IMP. Establish production plan, distribution plan and IRT settings for the start of the study
  • Provides input to protocol content, country selection and clinical risk databases
  • Defines or selects packaging configuration and labeling strategy
  • Coordinates an optimal IMP distribution strategy to ensure timely delivery to clinical sites
  • Uses project management techniques to manage effectively and efficiently the set-up of assigned phase 1-4 trials, or the set-up of new capabilities for CTS
  • Creates and maintains project plans, defining and achieving through the lead of cross functional teams the planned milestones regarding clinical supply set-up activities including packaging, labeling, distribution, Interactive Response Technology (IRT) and other supply systems.
  • Ensures Clinical Supply Lead visibility on study supply set-up activities for assigned trials, proactively identifying risks and escalating issues
  • Contributes to IRT specification development by defining the requirements for IMP/inventory management. Coordinates and/or participates in User Acceptance Testing.
  • Issues or coordinates availability of supply set-up documents
  • Ensures timely and cost effective supply availability for study start

Profile:

  • Master or Bachelor degree in Life Sciences.
  • Minimum of 2 years of Supply Chain expertise
  • Experience in Clinical Trials will be considered as an asset
  • Analytical mindset
  • Project Management experience (in a leading function)
  • Results oriented
  • Gathering and interpreting information
  • Leading others
  • Fluent in English

 Apply Now

Don't forget to mention EuroPharmaJobs when applying.

Share this Job

More Job Searches

Belgium     Manager and Executive     Manufacturing and Logistics     CROMSOURCE    

© EuroJobsites 2019

EuroJobsites is a UK registered company number: 4694396 VAT number: GB 880 9055 04

Registered address: EuroJobsites Ltd, Unit 8, Kingsmill Business Park, Kingston Upon Thames, London, KT1 3GZ, United Kingdom

Newsletter | Recruit | Advertise | Privacy | Contact Us

© EuroJobsites 2019

EuroJobsites is a UK registered company number: 4694396 VAT number: GB 880 9055 04

Registered address: EuroJobsites Ltd, Unit 8, Kingsmill Business Park, Kingston Upon Thames, London, KT1 3GZ, United Kingdom

This website uses cookies to make your experience better. Continued use of this website means you accept our cookie policy.  Accept Cookies