Irt Expert - Stuttgart, Deutschland - GULP Information Services GmbH

GULP Information Services GmbH

Geprüftes Unternehmen

Stuttgart, Deutschland

vor 3 Tagen

Geschrieben von:

Lena Wagner

beBee Recruiter

Das dürfen Sie erwarten:

Ihre Aufgaben:

Lead all activities consisting of assessment, planning, conceptual realization and implementation, as well as review, maintenance and decommissioning of studyspecific IRT concepts
Act independently as an IRT representative in crossorganizational and crossfunctional study and project teams and have deep expertise in the technical implementation of IRT concepts and clinical study design related to compliance and drug safety
Contribute to the continuous development of IRT concepts by bringing in new approaches and solutions to keep systems state of the art
Ensure that all work is performed with patient safety in mind and in compliance with GMP and GCP as well as US, EU and other international guidelines

Unsere Anforderungen:

Master's Degree in Natural Sciences and several years experiences in a related scientific discipline or Bachelor's Degree with long term experience in a related field
Experience in the IRT field, demonstrated indepth knowledge of the technical aspects and functions of an IRT system
Good understanding of global investigational drug activities, as well as general clinical trial execution and design
The ability to independently initiate and analyze complex tasks, taking into account applicable regulations, cost effectiveness, and timelines
Excellent communication skills and fluent in written and spoken English