Clinical Trial Administrator (f/m/d)

Clinical Trial Administrator (f/m/d)

Randstad Deutschland GmbH & Co. KG

Lokalizacja

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Position als Clinical Trial Administrator in der Pharmaindustrie in Biberach. Aufgaben: Planung, Management und Unterstützung bei klinischen Studien. Anforderungen: Bachelorabschluss, Erfahrung in der pharmazeutischen Industrie, gute Englischkenntnisse.

Słowa kluczowe

Betriebswirtschaft
Pharmaindustrie
Projektmanagement
US und EU Vorschriften
Microsoft Office 365
Kommunikationsfähigkeiten
Reisebereitschaft

Benefity

  • Zielgerichtetes Gehaltspaket
  • Umfangreiche soziale Leistungen
  • Bonuszahlungen zu Weihnachten und Feiertagen
  • Bis zu 30 Tage Urlaub pro Jahr
  • Vielfältige Mitarbeiterbenefits

Firmenbeschreibung

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: Our subsidiary Randstad professional solutions offers 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.

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 (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

Unsere Anforderungen

  • 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

Das dürfen Sie erwarten

  • 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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Wyświetlenia: 3
Opublikowana3 dni temu
Wygasaza 27 dni

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