Screen and enroll study subjects following the study protocol;
Collect samples from the study patients;
Maintain records of clinical data in CRF and send regularly to icddr,b head office;
Maintain documentation of all findings of study patients using standard data collection form and also assist the Project Coordinator to prepare documents related to patients;
Maintain excellent work relationship, coordination and linkages with other project staff;
Manage and solve any problems that may arise during the course of the study.