You should take a closer look at this: On behalf of our client in the pharmaceutical industry, we are looking for a motivated CTSU Distribution Assistance at the Biberach site. Could be a good fit, you say? Then apply quickly! And we mean "quickly" - just send us your name, e-mail address and CV. We'll get back to you as soon as possible and discuss everything else. We do not exclude anyone, but welcome every application.
Das dürfen Sie erwarten
* Attractive pay accoring to the BAP/DGB collective agreement
* Guaranteed punctual payment, possibility of installments
* Attractive social benefits, such as vacation and Christmas bonuses
* Good opportunities for takeover/employment at our client companies
* Up to 30 days vacation per year
* Representation of interests by a comprehensive works council
* Possibility to work from home up to 50% by arrangement
Ihre Aufgaben
* Support the Distribution Trial/Process Manager and IRT Trial/Process Manager for the autonomous management of CTSU supply change within the matrix structure within the organization and external vendors
* Planning the management and control of the schedule, cost and scope of global CTSU distribution for the agreed deliverables of global supply chain activities for assigned clinical trials, including highly complex studies
* Organization of meetings and their protocolization
* Collaboration in the documentation of the IRT and distribution system
* Maintenance of user lists for the IRT systems, administration of superuser access
* Creation and updating of POs
* Support in various systems, e.g. administration of workflows, EVA entries and updates
* Coordination of Elpro and IRT database evaluation and KPI collection
* Manual shipping request and release of forms
* Organization and monitoring of bulk shipments, stability samples and sampling documentation for investigational medicinal products
* Independently initiate and analyze complex tasks, taking into account applicable regulations, cost effectiveness and timelines
Unsere Anforderungen
* Successful Master's degree in natural sciences and several years of experience in a related scientific discipline or Bachelor's degree with many years of experience in a related field
* Good understanding of regulatory and GMP/GCP requirements in the pharmaceutical industry and their application to the function required
* Experience in the IRT field and proven in-depth knowledge of the technical aspects and functions of an IRT system an advantage
* Good knowledge of the general software development cycle, including validation of computer systems in the cloud desirable
* Fluency in written and spoken English
* Good understanding of global drug testing activities and the overall conduct and design of clinical trials
* Excellent communication skills