Randstad Professional
Clinical Trial Administrator (f/m/d)
Biberach an der Riß, Baden-Württemberg, Germany
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hirly's read of this role
- Role family
- Healthcare
- Seniority
- Mid level
- Stated salary
- €50,000 – €55,000 per year
- Country
- DE
- Work mode
- On-site / unstated
- First seen by hirly
- 15 Oct 2026
Derived automatically from the posting. Upload your resume above to see how the role scores against it.
the posting
- 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
- 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
Listed on hirly, a job board. hirly is not the employer: Randstad Professional is hiring for this role.
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