CTSU Trial Manager (f/m/d)
CTSU Trial Manager (f/m/d)
CTSU Trial Manager (f/m/d)
CTSU Trial Manager (f/m/d)
Randstad Deutschland GmbH & Co. KG
Pharma, Medizintechnik
Biberach, Baden
- Art der Anstellung: Vollzeit
- Vor Ort
CTSU Trial Manager (f/m/d)
Über diesen Job
CTSU Trial Manager (f/m/d)
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Vertragsart Arbeitnehmerüberlassung -
Einsatzorte 77781 Biberach, Baden -
Gehalt 60.000 - 70.000 EUR pro Jahr -
Beginn 18.08.2025 -
Arbeitszeitmodell Vollzeit
Ihr Ansprechpartner
Have you just completed your apprenticeship as a CTSU trial manager or would you like to reinvent yourself in a professional way? Our subsidiary Randstad professional solutions can help you! We are currently looking for a CTSU trial manager for a pharmaceutical company at our location in Biberach. Your passion for teamwork and your ability to learn quickly are the keys to an exciting new career! Apply now online! We value equal opportunities and welcome applications from people with disabilities.
Das bieten wir Ihnen
- Option of permanent employment with our business partner
- Extensive social benefits, incl. Christmas and holiday bonuses
- Up to 30 days vacation per year
- Free online courses, e.g. several language courses
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
Ihr Profil
- 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)
- German language skills, written and spoken
- Fluency in written and spoken English
- 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
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