Consultant for Evaluating the Operational Gains of the Master Facility Registry (MFR)

Job Description

Responsibilities & Key Deliverables
The consultant will be responsible for managing and delivering all components of Phase I. Key responsibilities and deliverables include:

Protocol Development and Regulatory ClearanceFinalize the research protocol
Secure ethical approval
Obtain official access letters from relevant institutions, including the Ethiopian Pharmaceutical Supply Service (EPSS) and Regional Health Bureaus
Desk ReviewCompare the legacy facility list with the MFR database to determine the number of duplicate or lack correct identification of facilities.
Analyze supply chain data to identify facilities previously receiving duplicate allocations
Qualitative Data Collection
Conduct key informant interviews (KIIs) with senior officials and program managers
Conduct key informant interviews across MoH directorates, EPSS, EPHI, regulatory units, and other relevant bodies
Assess usability, perceived and potential benefits of the MFR system
Preliminary Analysis and Dissemination

Conduct initial data analysis
Prepare and present preliminary findings from Phase I
About You
A minimum of Master’s degree in Public Health or a related field
Demonstrated experience in qualitative research design, data collection, and analysis
Strong skills in research methodology, report writing, and literature review
Solid understanding of standard research procedures and ethics
Proven ability to work independently and manage research activities
Track record of published research, reports, or academic work