Description du poste Mission and Responsibilities Reporting to the Data Management, IT, and Compliance Coordinator, the Data Manager (DM) will work closely with the other data managers and in collaboration with the study teams at Epicentre.

The Data Manager will be responsible for developing and maintaining clinical data management tools for research studies, ensuring the proper implementation, and maintaining the quality of data collected in compliance with ICH Good Clinical Practice (GCP) guidelines.

This applies to studies conducted at Epicentre’s research centers in Uganda and Niger and decentralized projects for which Epicentre oversees data management.   Main activities Develop and validate databases and data collection interfaces Develop data management plans for studies, SOPs, and other documentation related to data management  Ensure that all DM tools deployed in the different sites are up to date  Provide support to external partners and study sites on data management activities  Coordinate DM activities with the study site teams  Work with data controllers and clinical (or field) teams to follow up on daily data management tasks: data collection, visit planning, data entry, quality control, etc   Build tools for automatic and manual generation, identification and resolution of inconsistencies    Perform data review and report as required    Conduct data validation activities    Document clearly the technical details of the work to facilitate collaboration with other team members and ensure quality control    Conduct regular field visits in the countries where the studies sites are implemented    Reconcile study databases    Participate in data analysis and preparation of clinical study reports, publications, final reports, and presentations    Ensure archiving of study databases and related documents as needed   Support statisticians in the processes of statistical data analysis   Qualifications Diploma / professional training: Master's degree in computer science, Statistics or other similar fields with good programming skills Professional experience:     Minimum of 4  years of work experience in data Management.    Experience as a clinical trial data manager is an asset Skills: Clinical data management skills in clinical research contexts  Knowledge of research and methodology in clinical trials, good clinical practices, medical terminology, informatics, data protection, and reporting formats  Experience and/or knowledge of clinical data management tools (e.g.

REDCap, ODK, Comm Care, Open Clinica, etc.)  Strong written and verbal communication skills  Flexibility and ability to work in a team and under pressure  Fluency in English is mandatory.

fluency in french is a plus Informations supplémentaires What you will get You will work with a multicultural team in the field of epidemiology and clinical research You will evolve in the humanitarian environment Your contributions and ideas will be valued and highly appreciated You will participate in the life of the organization and your responsibilities will evolve over time Fixed-term contract of 12 months, renewable Position to start in January 2025  Position based in Uganda (Mbarara) with regular displacement to Niger reseach center and other study sites  Remuneration according to experience and Epicentre salary grid To apply Please send your application (CV + cover letter) no later than 21/10/2024 Only shortlisted applicants will be contacted.  At Epicentre, we are committed to an inclusive culture that encourages and supports the diverse voices of our employees.

We welcome applications from candidates regardless of gender, age, sexual orientation, nationality, ethnic origin, religion, beliefs, whether or not they have a disability, and all other diversity characteristics.

Epicentre pays very close attention to the protection of the personal data of its members, staff and people wanting to join the association.

The data collected during your application will be processed in a fair and high-quality manner, only by the staff in charge of recruitment, wherever in the world they may be working for an MSF entity.

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B.:   Female candidates meeting the application criteria are strongly encouraged to apply.