Coordinateur d'Étude – Essai INTEGRATE (H/F), Contrat à Durée Déterminée – 12 mois

• Coordinate a study team comprising clinicians, nurses, data monitor, data managers, data entry clerks…
• Ensure protocol compliance and GCP standards across the study site.
• Oversee implementation of study procedures and quality of data collection, in collaboration with the trial sponsor’s data management and monitoring team.
• Organize and deliver training for clinical and support staff on GCP, consenting procedures, protocol-specific procedures, and Lassa fever care practices.
• Ensure accurate and timely completion of Source Documents, Case Report Forms (CRFs) and other data tools.
• Supervise documentation and follow-up of adverse events (AEs) and serious adverse events (SAEs).
• Maintain and update the Investigator Site File (ISF).
• Support MSF project teams in developing and implementing retention strategies to avoid lost to follow-up.
• Prepare routine and ad hoc reports in compliance with study and sponsor requirements.
• Prepare and facilitate the site monitoring visits conducted by the trial oversight instances.
• Be a focal point for the study in MSF and provide regular updates/reports on the study progress to Epicentre, the PMR, the MSF medical coordination, and the LFTC MoH coordinator as requiredLiaise with Hospital/Ministry of Health members and with the INTEGRATE consortium members as needed
• Contribute to technical documentation, training tools, and job aids for health care workers and study team.
• Troubleshoot site-level issues related to human resources, equipment, or logistics, including liaison with Epicentre, MSF, and local authorities.
• Coordinate project closure activities and dissemination efforts.
• Uphold Epicentre and MSF’s ethical principles, including the respectful conduct of research in vulnerable populations.
• Perform other duties as required by the project and mission and in agreement with supervisors

• Medical degree (MD or equivalent) required. Specialization in Infectious Diseases or Intensive Care medicine is an asset.
• Degree in public health, epidemiology, or clinical research is a strong asset.
• Solid understanding of Good Clinical Practice (GCP).

• Required: Minimum of 3 years of experience implementing clinical trials in low-resource settings.
• Experience working as a clinician in viral hemorrhagic fever context is an asset.
• Experience working with MSF as a clinician is an asset.

• Excellent command of research project and team management – essential
• Excellent organizational, analytical, record-keeping, oral and written communication skills.
• 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 provide support / contribute beyond their area of expertise.
• Sense of responsibility, rigor.

• Fluently spoken and written English – C1 or above - essential
• French is an asset.

• Work in a multicultural team at the intersection of research and humanitarian medicine.
• Engage with MSF’s operational research agenda in a high-priority medical emergency.
• Be part of a mission-driven organization with a collaborative and supportive culture.

Epicentre