Clinical Supply Study Lead

91_6416

Obowiązki

o Study design input,

o Stakeholder management

o Demand & supply planning

o Cost management

o Compliance (GxP),

o Document creation (e.g., SSSD, SDPA),

o Risk management

o Packaging & distribution strategy

Wymagania

o Mid to senior-level of experience in clinical Supply Chain

o Experience inclinical trials management or supply chain experience in the pharmaceutical industry

o Knowledge of IRT systems

o Awareness of GXP Standards within a Clinical environment

o Project management and leadership skills

o Strong influencing, negotiating and problem solving skills across geographical/cultural boundaries and various stakeholders

o Demand planning and forecasting experience

o University degree (or equivalent) preferably in medical or biomedical science or discipline associated with clinical research

o English fluent written and spoken

Oferujemy

o Internal Mobility Program –enjoy many opportunities for career growth, job rotations, diversity of projects & technologies

o Referral Program –enjoy cooperation with your colleagues and get a bonus!

o 5/10 Years NATEK Club –we offer long-term cooperation and celebrate each fifth-year cooperation anniversary with gifts

o NATEK CSR Events & team buildings –enjoy our values: accountability, partnership and

expertise and #workITwithus

o Cafeteria

o Medical Healthcare

o Multisport Club Card

o Technical and Personal training

o Language courses

Additionally only for COW:

o Life insurance

o Bonuses for Personal Events

o Day off for volunteering

Źródło: Natek/Praca