(Poistunut julkaisusta)

Principal Data Manager
Bayer Oy

Alkuperäinen julkaisupäivä 16.4.2018

Bayer is now looking for an experienced and customer focused Principal Data Manager. This exciting and challenging role is a global role that is based in Espoo, Finland.


  • Lead the execution of data management activities  for Research and Development programs,  preparation of submission data and required documentation
  • Responsible for projects comprising of Phase I-IV trials (including project planning, resource allocation, progress tracking, management of external partners)
  • Act as key driver of the implementation and maintenance of consistent data management approaches across all studies within a development project, closely liaise with key interface functions
  • Mentor and coach study data managers assigned to respective project(s)
  • Support proactive data management specific project planning and tracking of assigned projects
  • Serve as key subject matter expert on topics related to data management activities, including specific activities and processes in early clinical development phases
  • Support the implementation of biomarker strategies for studies and projects, and organize the processes for pharmacokinetic data
  • Support research-driven activities incl. processing data provided by highly specialized functions; plan and manage data exchange processes between involved research and development functions
  • Ensure compliance with SOPs, GCP, ICH guidelines and the timely provision of high quality data for the use in early clinical development phases as well as in regulatory processes


  •  University Degree  in natural sciences, informatics or medical documentation
  • Long-term clinical study and/or project experience as a data manager in supportive and leading roles
  • Many years of experience as the data management lead  on clinical studies or projects
  • Significant experience of using data management methodologies and technologies (data warehousing, electronic data capture)
  • Understanding of data types typical for research activities and/or early phase development
  • Experience in using and programming databases and SAS
  • Demonstrated understanding of international drug regulations and guidelines (ICH, GCP, European Clinical Trials Directive, Privacy rules [HIPPA]) the drug development process
  • Strong self-management, organizational, communication and leadership skills
  • Source of inspiration and motivation for co-workers
  • Excellent written and oral English
  • Willingness to travel and flexible

We offer a competitive compensation, independent and challenging role in an international environment with a chance to develop your skills and experience further. To be considered for this exciting opportunity, please submit your application at your earliest convenience and no later than June 16th. Candidates will be reviewed on a continuous basis.

If you feel this unique role is just what you are looking for, we are keen to hear from you! For further information about the position, you are welcome to contact Luiz Giorgiani, Line Manager Global Data Sciences & Analytics, Global Clinical Development by mobile +358 400 807 868 and by e-mail luiz.giorgiani@bayer.com