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
experience in clinical trials
project management
regulatory requirements
GMP/GCP standards
MS Office
fluent English
good German skills
problem-solving skills
communication skills

Hexjobs Insights

Stanowisko: Menedżer prób klinicznych. Odpowiedzialność za działania łańcucha dostaw w badaniach klinicznych. Wymagana znajomość nauk przyrodniczych, doświadczenie w badaniach klinicznych oraz język angielski i niemiecki.

Schlüsselwörter

Master's degree in natural sciences
experience in clinical trials
project management
regulatory requirements
GMP/GCP standards
MS Office
fluent English
good German skills
problem-solving skills
communication skills

Vorteile

  • Wszystkie świadczenia socjalne, w tym premie świąteczne i urlopowe
  • Składka na fundusz emerytalny po zakończeniu okresu próbnego
  • Do 30 dni urlopu rocznie
  • Opcja stałej pracy u partnera biznesowego
  • Szeroka gama dodatkowych benefitów

Firmenbeschreibung

Our mission: We bring people together! Our subsidiary Randstad professional solutions is currently offering an attractive position as CTSU trial manager with one of our customers - a pharmaceutical company in Biberach. A fair compensation and personal support are of course included. You have a master's degree in natural science? Then you are a perfect match for us – we look forward to hearing from you! 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)
  • Fluent English and good German skills, both spoken and written
  • 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

  • Performance-based salary package depending on qualifications and professional experience
  • Extensive social benefits, incl. Christmas and holiday bonuses
  • Company pension scheme contribution after the end of the probationary period
  • Up to 30 days vacation per year
  • Option of permanent employment with our business partner
  • A wide range of employee benefits/perks

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Aufrufe: 1
Veröffentlichtvor etwa 11 Stunden
Läuft abin 30 Tagen
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