Randstad Professional
88400 Biberach an der Riß - Deutschland
Pharmazeut/in
Arbeit
Vollzeit
ab 10.03.2026
Beschreibung
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 sp... weiter lesen
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 sp... weiter lesen
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.
Time for change – time for a new job! You are a CTSU trial
manager and looking for a new professional challenge? Then stop
searching! We offer the job you are looking for: a secure job, fair
compensation and exciting new tasks at an attractive pharmaceutical
company in Biberach. 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
- Above-average salary
- Extensive social benefits, incl. Christmas and holiday bonuses
- Up to 30 days vacation per year
- Company pension scheme contribution after the end of the
probationary period
- Option of permanent employment with our business partner
- Definition of career goals
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.
Time for change – time for a new job! You are a CTSU trial
manager and looking for a new professional challenge? Then stop
searching! We offer the job you are looking for: a secure job, fair
compensation and exciting new tasks at an attractive pharmaceutical
company in Biberach. 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
- Above-average salary
- Extensive social benefits, incl. Christmas and holiday bonuses
- Up to 30 days vacation per year
- Company pension scheme contribution after the end of the
probationary period
- Option of permanent employment with our business partner
- Definition of career goals
Ref-Nr.: 9792536
Aktualisiert:
11.03.2026
Quelle: Bundesagentur für Arbeit
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Ob die Stelle noch verfügbar ist und weitere Informationen findest du direkt auf der Website der Bundesagentur für Arbeit. Bitte beachte: OPROMA ist nicht der Anbieter dieser Stelle und kann keine Auskünfte geben.
weitere Infos Rechtliche Hinweise zur Nutzung
Ob die Stelle noch verfügbar ist und weitere Informationen findest du direkt auf der Website der Bundesagentur für Arbeit. Bitte beachte: OPROMA ist nicht der Anbieter dieser Stelle und kann keine Auskünfte geben.
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