Job Responsibilities

  • Develops basic knowledge to evaluate and select the best potential Clinical site, Vendor.
  • Develops basic knowledge of contract, budget  and payment process with the Clinical Site, Vendor.
  • Collects documents from clinical site for the initial submissions both to the RA and LEC.
  • Plans, prepares, conducts and reports on-site/remote visits:  selection, initiation, monitoring, close-out in accordance with the protocol, SOP, the Local and the International regulations.
  • Demonstrates verbal and written proper communication with the Clinical site, study coordinator, Vendor, Project Manager, Sponsor
  • Collects and coordinates the project-required documents flow with the Clinical site, the RA, LEC, Vendor.
  • Communicates the project status to Project Manager and Team.
  • Coordinates payments to the Clinical site, Vendor.
  • Ensures own training program compliance and self-development.
  • Confirms performance of high Quality, Customer focus, Risk share, Teamwork.
  • Assumes Leading/Coaching  role  for the less experienced monitor(s) in the project. 
  • Required Education
  • Completed High education in Medicine or Pharmacy
  • Proficient command of written and spoken English

Required Experience

  • 3+ years of the independent monitoring