Summary
Date Posted: Friday, November 11, 2022 , Base Salary: Not Disclosed

JOB DETAILS:


Job Responsibilities:
• Report directly to Site trial Coordinator.
• Assist in insulin titration and monitoring of participant glycemic control.
• Ensure that participants return to clinic for appropriate intervals for collecting follow-up data (e.g., laboratory testing, completing surveys/questionnaires.
• Complete online study forms using a laptop computer or portable devices (e.g. iPad)
• After training, be able to activate and place Continuous Glucose Monitor (CGM) sensors, download sensor data, remove and replace with new sensor.
• Travel to study participants’ home every after specified interval to obtain CGM data.
• Distribute compensation payments to participants following each completed study milestone.
• Assist with recruitment and obtaining consent from participants
• Receive training and assist in the data collection for the qualitative (1:1 interviews), quality-of-life (surveys) and cost effectiveness sub-studies.
• Ensure the study is done according to the working protocol and adherence to the 1CH Guidelines of Good Clinical Practice (GCP).
• Maintain a close professional relationship with the government officials and other officials in the study area and at the study area.
• Work with the study coordinator and PI to ensure that the study-specific SOPs are complete and are updated regularly.
• Work in a professional and ethical manner with competence, accountability and integrity.
• Perform any other activities as may be assigned


Work Hours: 8

Experience in Months: 60

Level of Education: Postgraduate Degree

Job application procedure

If interested, please apply by sending a CV, over letter one page maximum and contact details of 3 references in English to jobapplication@tdatz.or.tz by the 18th of November, 2022; 1600 hours EAT. Please indicate the position you are applying for in the subject line. Only applications submitted via e-mail shall be considered.

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