Site Data Managera (SDM) benefits for Sponsor

  • reduce the administrative burden on the Principal investigator/Co-investigator =>
  • medical activities carried out in the visits, as required by the Protocol, can be given to =>
  • quality data from individual visits to the trial subjects enrolled in the source documentation
     
  • total time demands associated with the administration of clinical trials will not be a barrier to entry of clinical trial centers in the trial itself =>
  • SDM can Principal investigator/Co-investigator save up to 40% of the time that would otherwise be spent administrative

You interested in further information regarding the position of Site Data Manager? Contact us via the contact form or email, your questions are very pleased to answer.

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