Location: Uro care-AMBSO office, Kampala
Reporting to: Study Principal Investigator

Key Duties and Responsibilities:
• Overseeing the smooth running of clinical trials.
• Supervising and ensuring accurate and proper completion on enrollment activities, including informed.
• Ensuring that all requirements are available for smooth implementation of the study in a timely manner.
• Facilitating and monitoring of scheduling follow up, including auditing of case report forms
• Conduct coordination functions between departments of Laboratory, Pharmacy, Data, Community and clinical.
• Routinely review clinical records to ensure completeness.
• Track project activities to facilitate participant activity progress.
• Review, classify and make recommendations on all adverse events reported by the study team.
• Communicate with the study supervisor and PI to complete required action for reporting and management of adverse events and correct study forms for accuracy and completion daily.
• Communicate regularly with project leaders about study progress and issues through regular meetings.
• Conducting and attend regular study clinical staff meetings.
• Participate in the recruitment of study participants.
• Participate in staff training.

Essential Qualifications/ requirements:
• Bachelor’s degree in relevant sciences such as Public health, clinical medicine, nursing.
• A master’s of Science in Public Health, Research or related fields is also desirable.
• Up- To date practicing Licenses from respective licensing bodies.
• Prior experience working in a clinical trial is desirable
• Evidence of training in Good Clinical Practice (GCP) and Human Subject Protection (HSP).
• Excellent communication, organizational and interpersonal skills.