Randstad Professional
88400 Biberach an der Riß - Deutschland
Pharmazeut/in
Arbeit
Vollzeit
ab 13.01.2026
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.
Do you want to progress professionally and desire a job where you are
challenged and supported? With regular working hours, good benefits,
and diverse opportunities for further development? Then you've
come to the right place: We offer an attractive position as clinical
trial administrator for an attractive pharmaceutical company at
their location in Biberach. Apply online right away. We value equal
opportunities and welcome applications from people with 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 (e.g. Mega trials, adaptive trial design, digital trials,
trials fully outsourced to a third party (CRO) and Investigator
Initiated Studies (IIS), EAP as well as NPU programs)
- 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, manuel release form as well as
manuel shipping request for bulk shipments, stability samples and
sampling documentation for Investigational Medicinal Products
- Bachelor's Degree with some years of experience
- Relevant experience in 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
- Excellent written and verbal communication skills
- Willingness to travel
- Performance-based salary package depending on qualifications and
professional experience
- Extensive social benefits, incl. Christmas and holiday bonuses
- Up to 30 days vacation per year
- Candid corporate culture
- A wide range of employee benefits/perks
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.
Do you want to progress professionally and desire a job where you are
challenged and supported? With regular working hours, good benefits,
and diverse opportunities for further development? Then you've
come to the right place: We offer an attractive position as clinical
trial administrator for an attractive pharmaceutical company at
their location in Biberach. Apply online right away. We value equal
opportunities and welcome applications from people with 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 (e.g. Mega trials, adaptive trial design, digital trials,
trials fully outsourced to a third party (CRO) and Investigator
Initiated Studies (IIS), EAP as well as NPU programs)
- 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, manuel release form as well as
manuel shipping request for bulk shipments, stability samples and
sampling documentation for Investigational Medicinal Products
- Bachelor's Degree with some years of experience
- Relevant experience in 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
- Excellent written and verbal communication skills
- Willingness to travel
- Performance-based salary package depending on qualifications and
professional experience
- Extensive social benefits, incl. Christmas and holiday bonuses
- Up to 30 days vacation per year
- Candid corporate culture
- A wide range of employee benefits/perks
Ref-Nr.: 8648492
Aktualisiert:
12.01.2026
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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