Clinical Data Manager (m/f)

Baden Württemberg  ‐ Onsite
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Description


We are looking for a
Clinical Data Manager (m/f)

Reference: -en
Start: asap
Duration: 24 MM
Place: in Baden-Württemberg
Branch: Pharmazeutische Industrie

Your tasks:
  • Key liaison/data management lead to establish, align and confirm data management expectations for assigned trial(s)
  • Responsible for CDM trial level oversight
  • Build effective relationships with CROs/vendor partners
  • Review protocols and identify requirements for proper data capture including electronic case report form design and processing of clinical data ensuring accuracy, consistency and completeness
  • Oversee the design, creation and UAT plan and testing of clinical study databases along with development of edit check specifications and manual data listings as required
  • Define or review creation and maintenance of all essential data management documentation
  • Initiate and compile Trial Master File (TMF) relevant documentation containing the necessary CDM/Biostatistics & Data Sciences (BDS) documentation for a trial


Your qualifications
  • Bachelor's degree or Master's degree (e.g. MBA, MSc) with major/focus in Life Sciences, Computer Science, Statistics or similar
  • Experience clinical trial (data) management required
  • Initial experience within the pharmaceutical industry, CROs or academic sites
  • Technical expertise including industry data structure knowledge (e.g. CDASH/CDISC); EDC use and database specification experience
  • Experience in using Statistical Analysis Software (SAS) programming
  • Excellent in English



Skills:
- Clinical data manager
Start date
ASAP
Duration
24 MM
From
Hays AG
Published at
23.05.2017
Contact person:
Kerstin Werner
Project ID:
1348461
Contract type
Freelance
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