JOB DETAILS:

Duties Brief

• • Participate in study patient evaluations and management, informed consent procedures, initial and follow up visits for all illnesses.
  •  Ensure accurate and proper completion of all study logs and case record forms.
  •  Participate in organization and filing of study case record forms, and generation of reports in collaboration with the Study Coordinators and Data Management team.
  •  Participate in Adverse Event reporting activities.
  •  Perform clinical examinations and basic laboratory evaluations
  •  Provide appropriate treatment for participants
  • Provide guidance and support to junior staff such as clinical officers and nurses to develop and maintain their clinical practice
  • Maintain confidentiality of records and research findings as appropriate
  • Attend staff meetings
  • Maintain effective interpersonal relationships with other staff and participants

Qualification Required

• Study participants properly enrolled
• Study participants correctly evaluated and managed
•  Case record forms completed correctly
• Laboratory results entered in the case record forms
• Departmental and staff meetings attended