Our mission: We bring people together! We are currently offering an attractive position as CTSU trial manager with one of our customers - a pharmaceutical company in Biberach. A fair compensation and personal support are of course included. Do you have a master's degree in natural science? Then you are a perfect match for us - we look forward to hearing from you! We welcome applications from all suitably qualified persons regardless of any disabilities. Responsible for global Supply Chain activities for Investigational Medicinal Products (IMPs) of national and international Phase I-IV clinical trials in the Therapeutic Area General Medicine Function as the main point of contact to Clinical Operations and Clinical Development for assigned trials, ensuring the timely and cost efficient provision of clinical supplies Act as the responsible leader of the CTSU trial team within the matrix structure, ensuring cross-functional collaboration and development of interfaces for all Supply Chain activities on the basis of business, regulatory and industry needs Provide input to clinical trial protocols and bulk demands incl. comparator and non-IMP commercial products, to specific packaging designs and efficient distribution strategies Support investigations as Subject Matter Expert for assigned trials
- Master's degree in natural sciences or similar disciplines or completed vocational training with experience in clinical trials
- Several years experiences in clinical trial supplies or related business
- Experience in working in an international environment, as well as team leading and project management experiences
- Ideally good knowledge and understanding of the regulatory and GMP/GCP requirements for IMPs
- Ability to interpret complex project requirements
- Good software skills (MS Office)
- Fluent English and good German skills, both spoken and written
- Strong problem solving capabilities with the willingness to make decisions and the ability to drive results
- Very good communication, negotiation and presentation skillsAbility to work independently as well as in a team
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Clinical Trial Manager (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
