Drug Supply Trial Manager (m/f)

REFERENZNUMMER:

332531/11

IHRE AUFGABEN:

-Plan, drive and coordinate global DSM activities on a trial level during study set-up, as well as for non-IRT studies during trial conduct
-Ensure the right drug always gets to the right patient on time
-Define and advise the CTT on the optimal study supply strategy in terms of packaging design, technical and timeline feasibility, cost efficiency and risk management
-Provide complete and accurate clinical trial demand information using defined DSM processes and systems
-Coordinate trial deliverables within DSM and all other relevant associated functions
-Ensure that a trial-level project plan is developed together with all relevant roles and progress of deliverables adequately tracked
-Maintain proactive communication with internal customers such as CDM, SCM, OM, CSDS and MDM on trial changes and progress of deliverables
-Review clinical trial protocol and protocol amendments and provide input to drug supply sections
-Develop optimal packaging design to match the study design and a supply plan optimized for cost, feasibility and overage

IHRE QUALIFIKATIONEN:

-University Degree with work experience
-Project management experience
-Stakeholder management experience
-Fluency in English
-Great communication skills

WEITERE QUALIFIKATIONEN:

Clinical trial assistant