
Clinical Trial Manager (f/m/d)
Randstad Deutschland GmbH & Co. KG
Status
Hexjobs Insights
Stanowisko: Menedżer prób klinicznych. Odpowiedzialność za działania łańcucha dostaw w badaniach klinicznych. Wymagana znajomość nauk przyrodniczych, doświadczenie w badaniach klinicznych oraz język angielski i niemiecki.
Schlüsselwörter
Vorteile
- Wszystkie świadczenia socjalne, w tym premie świąteczne i urlopowe
- Składka na fundusz emerytalny po zakończeniu okresu próbnego
- Do 30 dni urlopu rocznie
- Opcja stałej pracy u partnera biznesowego
- Szeroka gama dodatkowych benefitów
Firmenbeschreibung
Our mission: We bring people together! Our subsidiary Randstad professional solutions is 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. You have a master's degree in natural science? Then you are a perfect match for us – we look forward to hearing from you! Apply online now! We welcome applications from all suitably qualified persons regardless of any disabilities.
Ihre Aufgaben
- 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
Unsere Anforderungen
- 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 skills
- Ability to work independently as well as in a team
Das dürfen Sie erwarten
- Performance-based salary package depending on qualifications and professional experience
- Extensive social benefits, incl. Christmas and holiday bonuses
- Company pension scheme contribution after the end of the probationary period
- Up to 30 days vacation per year
- Option of permanent employment with our business partner
- A wide range of employee benefits/perks
| Veröffentlicht | vor 6 Tagen |
| Läuft ab | in 24 Tagen |
| Quelle |
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