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Fully Remote – USA
  • Independently lead clinical studies from database build to lock
  • Oversee eCRF design, edit check specifications, UAT, data review, data cleaning, SAE reconciliation, and database lock
  • Draft essential data management documents, including CCG, DMP, DTA, and more
  • Serve as the primary point of contact for sponsor clients, leading kickoff meetings and ensuring seamless collaboration
  • Work across Phases 1-4 in various therapeutic areas, including oncology
  • Utilize expertise in multiple EDC systems such as Medidata Rave, Veeva, and Medrio
  • Bachelor’s degree in Life Sciences or a related field
  • Proven experience in clinical data management, leading studies from start to finish
  • Strong knowledge of EDC systems and industry regulations
  • Excellent communication and leadership skills
Accepted file types: doc, docx, pdf, odt, Max. file size: 100 MB.