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Looking for provider for EU Data Management FSP

  • Clinical development and testing, clinical CRO, Regulatory services - CMC writing - medical writing, Consulting - strategy and development
  • Biopharmaceuticals
  • Europe
  • 07/31/2013

Description

We are seeking a provider to provide flexible resources. The provider must be located near the Basel/Freiburg region.
Scope (may expand):

- Build an electronic CRF including programming of eChecks/IVRS integration/custom functions/reports/listings
- Define and manage SDTM datasets, including SDTM annotated CRF/ESP data specifications/define.xml/draft and final SDTM specifications/SDTM datasets
- Case report summaries and patient profiles programming (raw & SDTM)

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