PHAST
Kardinal-Wendel-Str.16
D-66424 Homburg
Tel: +49 6841 / 98 48 90
Fax: +49 6841 / 98 48 950

Clinical Data Manger

Responsibilities:

  • perform data management tasks within Global Data Management for trials and projects
  • coordinate and monitor the progress of all DM tasks
  • responsible for the timelines and quality of the data
  • review edit checks and CRFs
  • carry out data cleaning activities
  • perform data quality surveillance of CRO deliverables
  • assure quality of data by establishing and administering of guidelines and standards for clinical data management.


Professional qualification:
  • Master/Diploma of Science
  • proven experience as Clinical Data Manager in the pharmaceutical or biotechnology industry
  • successfully completed multiple studies from beginning to end
  • providing a full scope of Data Management experience
  • Excellent knowledge of regulations and guidelines with regard to clinical development
  • knowledge of medical terminology is required
  • proficient with data management and EDC systems
  • good knowledge of CDISC, SDTM and SAS
  • basis knowledge of SQL is a plus
  • sound understanding of relational database design and proficient computer skills

Adequate knowledge of:
  • command of the English language, communication skills, both oral and written
  • project management skills
  • sound interpersonal skills
  • team player and problem solver with consensus building skills
  • organization, planning and coordination skills

You are:
  • detail-oriented
  • able to prioritize duties and responsibilities while handling multiple projects