Randstad is one of the world's leading talent companies with the ambition to be the world's most equitable and specialized talent company. Through our "partner for talent" corporate strategy, we find, develop and connect specialized talents with companies - worldwide, locally and always at a high speed. We build high-quality, diverse, and agile teams, while individuals can enjoy a rewarding career path with equitable opportunities.

Randstad Professional is one of Randstad's four specializations and focuses on the placement of specialists and managers in the future-oriented sectors of IT, Engineering, Life Science and Office.

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.

• 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 skills
• Ability to work independently as well as in a team

• 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