SOS

Clinical Research Associate, ИФАРМА

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  3. Clinical Research Associate, ИФАРМА

Описание

Responsibilities:
  • Site identification and feasibility
  • Site Visits: SQV, SIV, SMV, SCV
  • Site Visit Reports preparation
  • Pre-Visit and Follow-up letters to sites
  • CTA/Investigator contract negotiation
  • Study progress trackers completion
  • SS-TMF maintenance and archiving
  • SRP collection
  • Correspondence with sites
  • Training of Investigators
  • Study supplies inventory (request, on site, return)
  • IP inventory (request, on site, return)
  • ISF maintenance and archiving
  • Submissions to IEC
  • Participation in IM and Team Meetings
  • Co-monitoring and coaching of less experienced CRAs
  • Support to Project Management activities