OPROMA

DEIN NÄCHSTER SCHRITT

Clinical Trial Administrator (f/m/d)

comp 88400 Biberach an der Riß - Deutschland
Pharmazeut/in Arbeit Vollzeit ab 12.11.2026
Infos zum Berufsbild: Aufgaben, Gehalt & Karriere
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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 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: We offer 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

  • 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

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Bewerben

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Ref-Nr.: 14500070
Aktualisiert: 11.11.2026
Quelle: Bundesagentur für Arbeit
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