Research Study Coordinator

7 May 2026 Research Study Coordinator at CIDRZ

• Leads day to day study operations, and ensure protocol adherence, compliance and data quality. • Coordination of study team members in collection of high quality in accordance to the study protocol. • Contributes to the development of standard operating procedures (SOPs) and training materials for study staff. • Responsible for training of study staff, providing leadership and coordinating across multiple components of the study. • Coordinates the piloting of the study in selected public health facilities. • Supports the study team in pre-study sanitization and study data dissemination activities. • Manages the day to day operations of recruitment, randomization, and follow-up. • Oversees the Informed Consent process, ensuring participants fully understand the nature of the study. Oversee data collection activities, quality assurance, quality control to ensure high- quality data outputs. • Oversees participant safety, confidentiality, monitoring of potential adverse events, protocol deviation and violations and timely reporting to relevant authorities. • Coordinates day to day collaboration, and communication between the study team and Principal Investigators. • Tracks study progress against set targets making sure the study is implemented within timelines, trouble shoot for any challenges and bottlenecks that may be encountered. • Engages and maintains strong partnerships with Ministry of Health at provincial, district and facility levels and other partners. • Prepares study reports, presentations for Principal Investigators, NHRA, UNZABREC and other study partners. • Full Grade 12 Certificate • Minimum Bachelor’s degree in health-related field.