How do they match: Clinical Data Managers

  • Contribute to the compilation, organization, and production of protocols, clinical study reports, regulatory submissions, or other controlled documentation.
  • Evaluate processes and technologies, and suggest revisions to increase productivity and efficiency.
  • Monitor work productivity or quality to ensure compliance with standard operating procedures.

  • Collaborate with others to determine design specifications or details.
  • Communicate project information to others.
  • Train others in computer interface or software use.