For our Global Supply Chain Department (Clinical Trial Supply) in Marburg we are currently looking for a
Senior Study Manager (m/f/x) Clinical Trial Supply
R 249007
Fulltime / Permanent
The Clinical Trial Supply (CTS) Senior Study Manager is responsible for managing the end to end supply chain for assigned clinical studies throughout the multi year study lifecycle. The CTS Senior Study Manager independently leads clinical studies to ensure compliant, on time supply of study medication and ancillary materials for our patients. Responsibilities include determining kit design and blinding, forecasting demand of investigational product and ancillary supplies, establishing and managing the depot network and distribution to clinical sites, and ensuring final return and destruction. The CTS Senior Study Manager also leads process improvement projects for the clinical supply chain and may have direct reports.
Tasks & Responsibilities:
1. Gives input to and oversees the implementation and execution of multi year clinical supply strategies and plans for assigned simple to complex clinical studies. Gathers and documents requirements for clinical supplies. Influences the protocol design for clinical supply reliability and efficiency. Leads demand forecasting for study(ies); leverages simulation and optimization tools capabilities to optimize clinical supply plans and minimize the effect of inherent uncertainties; adjusts plans monthly based on actual consumption and changes to clinical and/or supply assumptions; confirms supply plans
2. Presents IMP related CTS topics in Study Execution Teams, Clinical Development Teams and Product Development Expert Team/Chemistry, Manufacturing, & Controls Team. Determines labelling and clinical kit design based on protocol and countries needs; implements pooling concepts in the study
3. Establishes and monitors global network of regional and global depots to distribute drug supplies and ancillary supplies to countries and sites in assigned clinical studies. Coordinates timely and compliant importation and supply of drug supplies and ancillary supplies into regional and global depots. Manages the inventory levels and product expiry
4. Develops clinical trial supply documents and training to support study execution for clinical sites and patients (e.g. Investigational Medicinal Product (IMP) Manuals, product preparation and administration videos). Trains external stakeholders (i.e,. clinical monitors, clinical site personnel) and internal global clinical study teams regarding IMP handling
5. Utilizes Interactive Response Technology (IRT) systems to ensure reliable and efficient clinical supply to depots and sites. Co develops IRT specifications for drug supply management, participates in user acceptance testing and establish