Responsible for overall coordination of the MK8527 Study functions; clinical, pharmacy, counseling, recruitment, retention, and home visits.
Responsible for developing work plans and implementation schedules, and ensuring that the study’s aims and objectives, including recruitment, follow up, retention, and adherence, are achieved.
Performs clinical study procedures
Primarily responsible for managing and reporting adverse events.
Provides protocol guidance to staff and is responsible for developing standard operating procedures (SOPs) for the study.
Responsible for study related outreach activities, sensitization of the communities and liaising with the Community Advisory Group.
Coordinates study related communications and regulatory boards
Ensures submission of study progress and performance reports to the Principal Investigator.
Attends study meetings
Performs other duties as assigned by the Principal Investigator