Reports to: Study Coordinator
Period: 6 months
POSITION SUMMARY:
The primary function of this position is to implement day to day activities of the study in compliance with the study protocol.
Key Responsibilities
Screen and recruit potential study participants
Perform consenting procedures for all study participants
Conduct interviews for the study participants using the study data collection tools
Conduct any clinical assessments as required by the study protocol and tools
Ensure study data collection tools are completed with utmost accuracy and transmitted to the Study Coordinator for safe storage
Track all participants enrolled in the study and conduct phone and community tracing for those who miss appointments
Refer study participants to facility clinical teams and Study Coordinator as appropriate
Required Minimum Qualifications & Experience:
At least diploma-level qualification in a health related field
At least 2 years’ research experience
Good written and verbal communication skills in English and Kiswahili
Basics skills in computer software packages
Ability to work independently with minimal supervision
Experience in conducting qualitative research is an advantage
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