To handle and administer RUTF treatment according to the agreed protocol;
Accountability of RUTF;
To ensure all RUTF products are handled in accordance to GCP;
To ensure all RUTF related data are filled in the trial documents accurately; and
To perform any other study-related duty as may be advised by supervisors

QUALIFICATION AND COMPETENCE

A Diploma or degree in pharmacy from recognized training institution and holding a practicing license from pharmacy council;
At least two or more years work experience in clinical research;
Excellent written and oral communications skills in Kiswahili and English;
Computer literacy; and
Good Clinical Practice (GCP) training

TERMS OF SERVICE:

One year contract which may be renewed on the basis of performance and mutual agreement.

DUTY STATION:

The successful candidate will be based at NIMR Mwanza Centre and regularly visits at study sites.

COMPENSATION:

A competitive salary will be offered to the successful candidate as per project budget.