Randstad Professional
88400 Biberach an der Riß - Deutschland
Pharmazeut/in
Arbeit
Vollzeit
ab 11.02.2026
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 clinical trial
administrator and looking for a new professional challenge in
a pharmaceutical company? Then stop searching! We offer the job you
are looking for: Our subsidiary Randstad professional solutions offers
a secure job, fair compensation and exciting new tasks at an
attractive company in Biberach. Apply online now! We welcome
applications from all suitably qualified persons regardless of any
disabilities.
- Support of planning, managing and steering of timelines, costs and
scope of Trial Teams for agreed deliverables of global supply chain
activities for assigned clinical trials, including highly complex
trials
- Responsible to support Trial Managers for
the autonomous management of
the CTSU trial team within the matrix structure
- Support of CTS preparation documentation
- Support
of team meetings, minutes with action points and responsibilities
- Support of different systems like BIRDS (BI System) administration
and workflows, Focus entries/updates, CES entries/updates, AC
Evaluation coordination, AC Ordering, MLT drafting prior to TrM
review/approval, GTL maintenance etc.
- Support manuel shipping requests for bulk shipments, stability
samples and sampling documentation for Investigational Medicinal
Products
- Bachelor's degree with some years of experience
- Relevant experience in the pharmaceutical industry
- Basic project management skills
- Broad and thorough knowledge and understanding of applicable US and
EU regulations and other international regulations
- Strong problem solving capabilities and encourage the
implementation of innovative approaches, new technologies and
strategies to support the successful completion of supply chain
activities
- Proven ability to drive results in a changing environment and to
discuss and present proposals in a concise and effective manner
- Strong computer skills (e.g. Microsoft Office 365, Project
Management Software)
- Ability to present projects/status reports to different audiences
- Very good to fluent in English, spoken and written
- Willingness to travel
- Performance-based salary package depending on qualifications and
professional experience
- Option of permanent employment with our business partner
- Company pension scheme contribution after the end of the
probationary period
- A wide range of employee benefits/perks
- 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 clinical trial
administrator and looking for a new professional challenge in
a pharmaceutical company? Then stop searching! We offer the job you
are looking for: Our subsidiary Randstad professional solutions offers
a secure job, fair compensation and exciting new tasks at an
attractive company in Biberach. Apply online now! We welcome
applications from all suitably qualified persons regardless of any
disabilities.
- Support of planning, managing and steering of timelines, costs and
scope of Trial Teams for agreed deliverables of global supply chain
activities for assigned clinical trials, including highly complex
trials
- Responsible to support Trial Managers for
the autonomous management of
the CTSU trial team within the matrix structure
- Support of CTS preparation documentation
- Support
of team meetings, minutes with action points and responsibilities
- Support of different systems like BIRDS (BI System) administration
and workflows, Focus entries/updates, CES entries/updates, AC
Evaluation coordination, AC Ordering, MLT drafting prior to TrM
review/approval, GTL maintenance etc.
- Support manuel shipping requests for bulk shipments, stability
samples and sampling documentation for Investigational Medicinal
Products
- Bachelor's degree with some years of experience
- Relevant experience in the pharmaceutical industry
- Basic project management skills
- Broad and thorough knowledge and understanding of applicable US and
EU regulations and other international regulations
- Strong problem solving capabilities and encourage the
implementation of innovative approaches, new technologies and
strategies to support the successful completion of supply chain
activities
- Proven ability to drive results in a changing environment and to
discuss and present proposals in a concise and effective manner
- Strong computer skills (e.g. Microsoft Office 365, Project
Management Software)
- Ability to present projects/status reports to different audiences
- Very good to fluent in English, spoken and written
- Willingness to travel
- Performance-based salary package depending on qualifications and
professional experience
- Option of permanent employment with our business partner
- Company pension scheme contribution after the end of the
probationary period
- A wide range of employee benefits/perks
- Definition of career goals
Ref-Nr.: 9258511
Aktualisiert:
10.02.2026
Quelle: Bundesagentur für Arbeit
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.
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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