Job Role / Responsibilities:
You will be responsible to:
develop and maintain a strong understanding of the study protocol and related study instrumentsliaise and coordinate study requirements with relevant units and departments of the institution in line with AKU institutional policiesperform clinical assessments and provide medical care to study subjects, including initial screening for eligibility, prescribing study medications, and ongoing assessments and follow-upsorganise and/or administer the informed consent process in conjunction with the principal investigatorcoordinate and provide patient care in compliance with protocol requirements, including patient screening, recruitment, scheduling, and study visit procedureswhere relevant, disburse investigational products upon written authorisation from the PI and provide appropriate guidance on their administrationmaintain study documentation as per protocol...