Clinical Trial Supply Manager – Novartis Drug Supply Management (NOVJP00025517) (m/f)

REFERENZNUMMER:

362845/11

IHRE AUFGABEN:

-Represent DSM as a core member in the integrated Clinical Trial Team (iCTT); define and advise the iCTT on the optimal clinical trial supply strategy in terms of, but not limited to, packaging design, technical and timeline feasibility, efficiency and risk management
-Review overall clinical trial protocol/protocol amendments, provide input to develop optimal packaging design, clinical trial supply design and visit schedule
-Create and maintain complete and accurate clinical supply demand for assigned study in alignment with protocol requirements, key study parameters and milestones, patient projections, with appropriate overage and by using defined processes and systems
-Create and drive finalization of the packaging design (Clinical Packaging Request) and a comprehensive label strategy for all participating countries in the clinical trial

IHRE QUALIFIKATIONEN:

-Degree in science, engineering or equivalent
-Fluency in English
-Good expertise in related field
-Good knowledge about the drug development process
-Basic project management skills, good organization and planning skills
-Knowledge of relevant regulations (e.g. GMP, HSE etc.) and Novartis specific standards
-Very good communication, negotiation and interpersonal skills
-Ability to work in interdisciplinary teams

WEITERE QUALIFIKATIONEN:

Clinical project manager