Job Description
NATEK is hiring aClinical Supply Study Lead to join an international company and leadsupply chain for global clinical trial studies across all phases within drug development.
Your Responsibilities
- Study design input,
- Stakeholder management
- Demand & supply planning
- Cost management
- Compliance (GxP),
- Document creation (e.g., SSSD, SDPA),
- Risk management
- Packaging & distribution strategy
Our Requirements
Mid to senior-level of experience in clinical Supply ChainExperience inclinical trials management or supply chain experience in the pharmaceutical industryKnowledge of IRT systemsAwareness of GXP Standards within a Clinical environmentProject management and leadership skillsStrong influencing, negotiating and problem solving skills across geographical / cultural boundaries and various stakeholdersDemand planning and forecasting experienceUniversity degree (or equivalent) preferably in medical or biomedical science or discipline associated with clinical researchEnglish fluent written and spokenBenefits
Internal Mobility Program –enjoy many opportunities for career growth, job rotations, diversity of projects & technologiesReferral Program –enjoy cooperation with your colleagues and get a bonus5 / 10 Years NATEK Club –we offer long-term cooperation and celebrate each fifth-year cooperation anniversary with giftsNATEK CSR Events & team buildings –enjoy our values : accountability, partnership andexpertise and #workITwithus
CafeteriaMedical HealthcareMultisport Club CardTechnical and Personal trainingLanguage coursesAdditionally only for COW :
Life insuranceBonuses for Personal EventsDay off for volunteering