Time for change - time for a new job! Are you an IRT expert and looking for a new professional challenge? Then stop searching! We offer the job you are looking for: a secure job, fair compensation and exciting new tasks at an attractive pharmaceutical company in Biberach. We welcome applications from all suitably qualified persons regardless of any disabilities.
Develop IRT System specifications to meet the needs of the study design in collaboration with Clinical Trial Supply Unit (CTSU) functions, Medical, Clinical Data Management and Biostatistics Select IRT Vendor and create study specific contract Conduct and document Validation/User Acceptance Test activities Perform regular maintenance of the IRT system to adjust for trial needs, additional requirements after go-live etc, in collaboration with the study team Utilize agile and proactive approach and innovative technology to solve problems Support the successful setup of the supply chain and patient management activities through the use of IRT Ensure that all work is performed according to GxP and conforms with US, EU and other international regulations Work independently and in an international, cross-culture team environment
- Master's degree with several years of professional experience
- Proven ability to drive results in a changing environment and to discuss and present proposals in a concise and effective manner
- Ability to learn new technologies and concepts to enhance operations
- Strong problem solving capabilities and encouragethe implementation of innovative approaches, new technologies and strategies to support the successful completion of supply chain activities
- Exhibitability to interpret complex project requirementsand provideability to interpret highly complex experimental data and project requirements
- Solid project management skills including presenting projects and status reports to different audiences
- Fluent in English with excellent written and verbal communication skills
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IRT Expert (f/m/d) in Biberach an der Riss Arbeitgeber: GULP Information Services GmbH
Als Compliance Specialist (m/w/d) in unserem Standort Kassel profitieren Sie von einer dynamischen Arbeitsumgebung, die Präzision und Qualität in den Mittelpunkt stellt. Wir bieten Ihnen nicht nur ein attraktives Gehalt und umfassende Sozialleistungen, sondern auch zahlreiche Möglichkeiten zur beruflichen Weiterentwicklung in einem innovativen High-Tech-Umfeld. Unsere offene Unternehmenskultur fördert Teamarbeit und den Austausch von Ideen, sodass Sie als wertvolles Mitglied unseres Teams wachsen können.
Kontaktdaten:
GULP Information Services GmbH Recruiting-Team
