Time for change – time for a new job! Are you a clinical trial administrator and looking for a new professional challenge in a pharmaceutical company? Then stop searching! We offer the job you are looking for: We offer a secure job, fair compensation and exciting new tasks at an attractive company in Biberach. We welcome applications from all suitably qualified persons regardless of any disabilities. Support of planning, managing and steering of timelines, costs and scope of Trial Teams for agreed deliverables of global supply chain activities for assigned clinical trials, including highly complex trials Responsible to support Trial Managers for the autonomous management of the CTSU trial team within the matrix structure Support of CTS preparation documentation Support of team meetings, minutes with action points and responsibilities Support of different systems like BIRDS (BI System) administration and workflows, Focus entries/updates, CES entries/updates, AC Evaluation coordination, AC Ordering, MLT drafting prior to TrM review/approval, GTL maintenance etc. Support manual shipping requests for bulk shipments, stability samples and sampling documentation for Investigational Medicinal Products
- Bachelor's degree with some years of experience
- Relevant experience in the pharmaceutical industry
- Basic project management skills
- Broad and thorough knowledge and understanding of applicable US and EU regulations and other internationalregulations
- Strong problem solving capabilities and encouragethe implementation of innovative approaches, new technologies and strategies to support the successful completion of supply chain activities
- Proven ability to drive results in a changing environment and to discuss and present proposals in a concise andeffective manner
- Strongcomputerskills(e.g. Microsoft Office 365, Project Management Software)
- Ability to present projects/status reports to different audiences
- Very good to fluent in English, spoken and written
- Willingness to travel
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Clinical Trial Administrator (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
