Headquarters
Austria
Belgium
nl frde
Brazil
China
France
Germany
India
Italy
Korea
Lebanon
Netherlands
Poland
Russia
Singapore
Spain
Sweden
Switzerland
United Kingdom
USA
LATAM
MEA
SEA
Erbe Worldwide

Please choose a website and your preferred language.

For the Research and Basic Technologies Department of our Tübingen location, we are looking for a

Clinical Study Manager (m/f/d)


Your Responsibilities


  • Plan and implement preclinical and clinical studies; prepare clinical investigation plans, clinical study reports and scientific publications
  • Take on the role of Study Director in GLP studies
  • Select and interact with external vendors (e.g. CRO, EDC providers, preclinical laboratories)
  • Audit and monitor study centers, co-monitor and audit vendors
  • Carry out national and international preclinical and clinical studies according to MPG, GCP, GLP as well as relevant ICH and FDA guidelines. This will be done in cooperation with our interdisciplinary research team and the departments of quality management and marketing
  • Ensure that regulatory quality requirements are satisfied
  • Act as contact person for investigators, medical cooperation partners and non-medical staff

Your Skills


  • Successful completion of studies in human medicine, human biology or a similar scientific discipline
  • Professional experience in organizing preclinical and clinical studies; ideally several years of professional experience with preclinical GLP studies
  • Good understanding of regulatory requirements in the context of preclinical and clinical studies, ideally for medical device studies
  • You enjoy working with people, data and numbers in an international environment
  • Strong organizational and communication skills
  • You enjoy teamwork and flexibility
  • Prepared to travel
  • Fluent business English
Benefits:

  • Wide range of health management services, including cooking classes, health days, vaccination campaigns and fitness studio memberships
  • Electric car charging stations and free parking 
  • Challenging tasks and a lot of personal responsibility
  • Multicultural and international collaboration
  • Attractive monthly remuneration
  • Flexible working hours and the opportunity to work a hybrid schedule 
  • Onboarding with an introductory event and an individual induction plan as well as a wide range of internal and external training courses 
  • Social, societal and environmental responsibility

Are you interested?

If so, we look forward to receiving your application, including your salary expectations and the earliest possible starting date. Please apply via our career portal.