The Ugandan Jobline

• Participation in initiation, monitoring, and closeout visits in
  compliance with the approved protocol and study procedures;
• Communication with the research site staff (administrative and
  medical) including coordinators, clinical research physicians and
  laboratory staff.
• Tasked with verifying adequate investigator qualifications, training
  and resources, including facilities, laboratories, equipment, and staff.
• Ensure that the Investigator site file is up to date with the
  latest regulatory documents.
• Medical record and research source documentation verification
  against case report form data, including informing the site staff of any
  entry errors, ensuring good documentation practices are being adhered to
  and communicating protocol deviations appropriately per SOPs, GCP and
  applicable regulatory requirements

• The applicant must hold a University degree in a related health
  profession or a field related to research compliance.
• One year of experience in monitoring of clinical research.
• Knowledge of ICH guidelines, GCP, and the clinical trial study
  process.
• Ability to encompass knowledge of scientific concepts related to design
  and analysis of clinical trials
• Good report writing skills

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