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Clinical trial manager (f/m/d)

Biberach
GULP – experts united
Clinical Trial Manager
Inserat online seit: 8 August
Beschreibung

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.

Here's what we offer

1. Option of permanent employment with our business partner
2. Up to 30 days vacation per year
3. Extensive social benefits, incl. Christmas and holiday bonuses
4. Free online courses, e.g. several language courses

Your tasks

5. 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
6. 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
7. 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
8. Provide input to clinical trial protocols and bulk demands incl. comparator and non-IMP commercial products, to specific packaging designs and efficient distribution strategies
9. Support investigations as Subject Matter Expert for assigned trials

Your profile

10. Master's degree in natural sciences or similar disciplines or completed vocational training with experience in clinical trials
11. Several years experiences in clinical trial supplies or related business
12. Experience in working in an international environment, as well as team leading and project management experiences
13. Ideally good knowledge and understanding of the regulatory and GMP/GCP requirements for IMPs
14. Ability to interpret complex project requirements
15. Good software skills (MS-Office)
16. German language skills, written and spoken
17. Fluency in written and spoken English
18. Strong problem solving capabilities with the willingness to make decisions and the ability to drive results
19. Very good communication, negotiation and presentation skills
20. Ability to work independently as well as in a team

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