Job description


  • Entry level
  • No Education
  • Salary to negotiate
  • Dar es Salaam


Strategically focused on providing key local relational and operational support to investigative site personnel and CRAs, ensuring customer engagement, satisfaction and support to the clinical trials. The responsibilities include, but are not limited to: -Primary sponsor point of contact for site personnel relative to clinical trial related issues. -Influence the design of clinical study protocols including input on protocol and enrollment feasibility. -Identify, screen, evaluate and develop investigators for clinical trial participation. What is Required: (Qualifications, experience & Skills) -Science Degree. PhD will be evaluated very positively -Previous experience in Clinical Trials, at least as CTM -Experience in Neurology and / or immunology will be positively valued -Personal Skills: Communication, Proactive, Accountability & Delivery, Team player -Good written and spoken English -Computer literacy: Microsoft Word, Excel, PowerPoint, Outlook.

  • excel
  • powerpoint
  • protocol
  • word