Study Coordinator

Location

Contract Type

Qualification Required:

MASTERS : MBChB/MD - Mandatory
MSc in Epidemiology, Biostatistics or related field (Added Advantage) - Added Advantage
2–3 years' research experience - Optional

Responsibilities:

1. Lead and coordinate the implementation of all AVERT study activities across designated study sites, ensuring adherence to study protocols, timelines, and quality standards.
2. Plan and conduct sensitization meetings with district leaders, health facility staff, and other key stakeholders to facilitate successful study implementation.
3. Coordinate study activities at designated Malaria Reference Centres (MRCs) and ensure effective collaboration with health facility teams.
4. Liaise with the PRISM surveillance team to harmonize health facility-based and cross-sectional survey activities for the AVERT study
5. Develop work plans, activity schedules, and budgets to support timely implementation of field activities
6. Participate in the development, review, and implementation of study protocols, Standard Operating Procedures (SOPs), data collection tools, and other study documentation
7. Train, mentor, and provide continuous medical education (CMEs) to study clinicians and health facility staff to ensure compliance with study procedures and Good Clinical Practice (GCP)
8. Conduct routine monitoring visits and data quality assessments to ensure accuracy, completeness, and integrity of study data
9. Oversee the informed consent process, participant screening, enrolment, and follow-up in accordance with approved study protocols and ethical guidelines.

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