STUDY COORDINATOR – PAVE POST-THERMAL ABLATION FOLLOW-UP STUDY

Responsabilités

OVERVIEW Médecins Sans Frontières (MSF) is an independent, non-profit international humanitarian organisation that provides medical assistance to populations affected by crises, regardless of race, religion, creed, or political affiliation. In Malawi, MSF collaborates with the Ministry of Health and local communities, particularly through its cervical cancer project in Blantyre and Chiradzulu districts, as well as the CBO Project in Zalewa and Dedza District. MSF France is recruiting a Study Coordinator to coordinate the field implementation of the PAVE Post-Thermal Ablation Follow-up Study in Malawi. The study aims to assess outcomes among women previously screened for cervical cancer, particularly those who underwent thermal ablation or were diagnosed with CIN2+. The successful candidate will coordinate study activities from set-up to closure, ensuring quality, ethical conduct, compliance with the study protocol, and reliable data collection. The role will also involve participant follow-up, clinical coordination, and collaboration with MSF, Epicentre, and participating health facilities. JOB TYPE: Fixed-term contract CONTRACT DURATION: 9 months START DATE: As soon as possible SALARY: Level 12 of the MSF field salary grid, plus benefits linked to the field contract Application Deadline: Sunday, 1st November, 2026, at 5:00 PM POSITION: STUDY COORDINATOR KEY REQUIREMENTS Academic, Professional Qualifications and Experience Applicants should possess the following qualifications and experience: A degree in Public Health, Epidemiology, or Clinical Research. Alternatively, a medical or paramedical qualification, such as a degree in medicine, midwifery, or nursing, with sufficient clinical experience to review and interpret medical records and understand clinical pathways. A solid understanding of Good Clinical Practice (GCP). Demonstrated experience implementing and coordinating epidemiological, operational, or clinical research. Experience in project coordination and team management is essential. Experience in sexual and reproductive health, women's health, cervical cancer prevention, or HPV screening and treatment is a strong advantage. Experience reviewing and extracting information from medical records and clinical documentation is an advantage. Experience in cohort studies, longitudinal follow-up, or research involving active participant tracing is an advantage. Experience working with MSF, Ministry of Health services, or similar health programmes is an advantage. Language Requirements Fluency in spoken and written English. Knowledge and Skills: Excellent research project and team management skills. Strong organisational, analytical, and record-keeping skills. Excellent oral and written communication skills. Personal Specification: The successful candidate should demonstrate: Ability to adapt to complex and changing environments and meet tight deadlines. Collaborative and inclusive leadership. Strong interpersonal skills, team spirit, and diplomacy. Ability to support and contribute beyond their immediate area of expertise. A strong sense of responsibility and attention to detail. DUTIES AND KEY RESPONSIBILITIES The Study Coordinator will be responsible for the following: Coordinating the overall field implementation of the study, from set-up to closure, including planning, monitoring, and adapting study activities in line with the protocol, standard operating procedures (SOPs), timelines, ethical requirements, and Good Clinical Practice. Coordinating and supervising the study team, including nurses, community health workers, and the driver, in collaboration with MSF and Epicentre. Ensuring appropriate staff training on the study protocol, SOPs, research ethics, confidentiality, study procedures, and data collection. Overseeing study data management and quality, ensuring accurate and timely completion of study forms and electronic databases. Conducting regular checks for data completeness and consistency, resolving data queries, and ensuring secure handling of participants' identifiable information. Maintaining essential study documentation and implementing quality-control and monitoring procedures. Identifying and reporting protocol deviations or issues affecting participant safety, ethical conduct, or data quality. Monitoring study progress and addressing operational challenges related to participant follow-up, human resources, clinical coordination, data, equipment, transport, and logistics. Serving as the main field

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