
Clinical Trial Administrator (f/m/d)
Randstad Deutschland GmbH & Co. KG
Status
Hexjobs Insights
Poszukiwana osoba na stanowisko administratora badań klinicznych w Biberach. Wymagana znajomość regulacji i umiejętności zarządzania projektami. Oferowane stałe zatrudnienie oraz atrakcyjne benefity.
Schlüsselwörter
Vorteile
- Zatrudnienie na podstawie stałej umowy
- Składka na fundusz emerytalny po okresie próbnym
- Szeroki wachlarz benefitów dla pracowników
- Możliwość określenia celów zawodowych
Firmenbeschreibung
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.
Ihre Aufgaben
- 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
Unsere Anforderungen
- 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
Das dürfen Sie erwarten
- 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
| Veröffentlicht | vor 23 Tagen |
| Läuft ab | in 7 Tagen |
| Quelle |
Ähnliche Jobs, die für Sie von Interesse sein könnten
Basierend auf "Clinical Trial Administrator (f/m/d)"
Keine Angebote gefunden, versuchen Sie, Ihre Suchkriterien zu ändern.