Clinical Trial Manager (f/m/d)
Clinical Trial Manager (f/m/d)
Clinical Trial Manager (f/m/d)
Clinical Trial Manager (f/m/d)
Randstad Deutschland GmbH & Co. KG
Pharma, Medizintechnik
Biberach an der Riß
- Art der Anstellung: Vollzeit
- Vor Ort
- Zu den Ersten gehören
Clinical Trial Manager (f/m/d)
Über diesen Job
Clinical Trial Manager (f/m/d)
-
Vertragsart Arbeitnehmerüberlassung -
Einsatzorte 88400 Biberach an der Riß -
Gehalt 60.000 - 70.000 EUR pro Jahr -
Beginn 15.10.2025 -
Arbeitszeitmodell Vollzeit
Job ID C01169814 Veröffentlicht am 08.08.2025 00:30
Ihr Ansprechpartner
Frau Sarah Fekete +49 731 3793518
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. 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.
Das bieten wir Ihnen
- Option of permanent employment with our business partner
- Up to 30 days vacation per year
- Extensive social benefits, incl. Christmas and holiday bonuses
- 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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