Clinical Trial Manager (f/m/d)

Clinical Trial Manager (f/m/d)

Randstad Deutschland GmbH & Co. KG

Standort
Biberach an der Riß
Master's degree in natural sciences
clinical trial supplies
project management
negotiation skills
GMP/GCP knowledge

Hexjobs Insights

Poszukiwany CTSU trial manager w Biberach. Odpowiedzialność za globalne działania łańcucha dostaw produktów medycznych w badaniach klinicznych. Wymagana: wykształcenie wyższe, doświadczenie w trialach.

Schlüsselwörter

Master's degree in natural sciences
clinical trial supplies
project management
negotiation skills
GMP/GCP knowledge

Vorteile

  • Opcja stałego zatrudnienia
  • Rozbudowane benefity socjalne, w tym premie świąteczne i urlopowe
  • Do 30 dni urlopu w roku

Firmenbeschreibung

Time for change – time for a new job! You are a CTSU trial manager and looking for a new professional challenge? 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 pharmaceutical company in Biberach. Apply online now! We welcome applications from all suitably qualified persons regardless of any disabilities.

Ihre Aufgaben

  • Responsible for global Supply Chain activities for Investigational Medicinal Products (IMPs) of national and international Phase I-IV clinical trials in the Therapeutic Area General Medicine
  • Function as the main point of contact to Clinical Operations and Clinical Development for assigned trials, ensuring the timely and cost efficient provision of clinical supplies
  • Act as the responsible leader of the CTSU trial team within the matrix structure, ensuring cross-functional collaboration and development of interfaces for all Supply Chain activities on the basis of business, regulatory and industry needs
  • Provide input to clinical trial protocols and bulk demands incl. comparator and non-IMP commercial products, to specific packaging designs and efficient distribution strategies
  • Support investigations as Subject Matter Expert for assigned trials

Unsere Anforderungen

  • Master's degree in natural sciences or similar disciplines or completed vocational training with experience in clinical trials
  • Several years experiences in clinical trial supplies or related business
  • Experience in working in an international environment, as well as team leading and project management experiences
  • Ideally good knowledge and understanding of the regulatory and GMP/GCP requirements for IMPs
  • Ability to interpret complex project requirements
  • Good software skills (MS-Office)
  • German language skills, written and spoken
  • Fluency in written and spoken English
  • Strong problem solving capabilities with the willingness to make decisions and the ability to drive results
  • Very good communication, negotiation and presentation skills
  • Ability to work independently as well as in a team

Das dürfen Sie erwarten

  • Option of permanent employment with our business partner
  • Extensive social benefits, incl. Christmas and holiday bonuses
  • Up to 30 days vacation per year

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Veröffentlichtvor 2 Tagen
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