Actively participated in USAID PEPFAR funded program transition from international to local NGO with demonstrated adaptability to new work environment. Result driven.

Contributed to build programmatic and financial capacity of local organizations based in East and Adamawa regons, that are partnering with NECC, strengthening their ability to better manage funds and deliver effective and efficient health programs.

Fluent in French and English. I have worked in monitoring evaluation accountability and learning field in UNHCR- and USAID- funded projects. I used quantitative and qualitative methods in Food security monitoring methodology (VAM), HIV related domains, health, mental health, protection, WASH, social cohesion, social services, Market assessment, Cash-Based-Transfer and livelihood: International experience both in the US, France and Cameroon. Demonstrated successful skills in Business… Show more Fluent in French and English. I have worked in monitoring evaluation accountability and learning field in UNHCR- and USAID- funded projects. I used quantitative and qualitative methods in Food security monitoring methodology (VAM), HIV related domains, health, mental health, protection, WASH, social cohesion, social services, Market assessment, Cash-Based-Transfer and livelihood: International experience both in the US, France and Cameroon. Demonstrated successful skills in Business Development (UNICEF and UNHCR projects). Experience in emergency preparedness in context of insecurity. Excellent skills in designing M&E system, as well as complex tool design and creation on Kobo/ODK/Commcare platforms and dashboard creation on Power Bi. Good scientific writing skills. Excellent Computer proficiency. Actively engaged in training and partners’ capacity strengthening. Supervisory role. Show less

Une premiere experience avec CRS incroyablement dense, dans le monde du suivi evaluation pour un projet OEV allant sur sa 5e et derniere annee, finance par le Fonds Mondial, avec au bout de 6 mois, un role de Acting Project Manager pendant 6 mois, en vue de cloturer avec succes un projet de 5 ans. Ce fut passionnant, riche en experience avec le support d'une armee de stagiaires tout aussi passionnes, abattant un travail de titans, motives et prets a s'engager a la fin de leur contrat, pour une… Show more Une premiere experience avec CRS incroyablement dense, dans le monde du suivi evaluation pour un projet OEV allant sur sa 5e et derniere annee, finance par le Fonds Mondial, avec au bout de 6 mois, un role de Acting Project Manager pendant 6 mois, en vue de cloturer avec succes un projet de 5 ans. Ce fut passionnant, riche en experience avec le support d'une armee de stagiaires tout aussi passionnes, abattant un travail de titans, motives et prets a s'engager a la fin de leur contrat, pour une autre aventure a l'Est Cameroun, dans d'autres projets avec CRS, cette fois, finances par le HCR, le PAM et qui changera leurs vies pour toujours, mais aussi la vie de ceux qu'ils servaient. Show less

PMTCT HIV context

•Data monitoring•Resolved queries and other data discrepancies.•SAE report

•Electronic Data Capture. •Familiar with Medical Devices. •Conducted research data management •Conducted statistical analyses of research data using Microsoft Excel and SPSS. •Created patient databases with secured network access (MS Access). •Resolved queries and other data discrepancies. •Prepared data tables for presentation to Principal Investigators. •Prepared posters for international scientific annual meetings. •Designed case report… Show more •Electronic Data Capture. •Familiar with Medical Devices. •Conducted research data management •Conducted statistical analyses of research data using Microsoft Excel and SPSS. •Created patient databases with secured network access (MS Access). •Resolved queries and other data discrepancies. •Prepared data tables for presentation to Principal Investigators. •Prepared posters for international scientific annual meetings. •Designed case report forms for pharmaceutical companies. •Conducted recruitment strategies and study visits: patient enrollment, screening and follow-up visits. •Prepared, reviewed, and submitted protocol and regulatory documents to IRB. •Proposed Trial Budgets. •Ensured protocol compliance reporting in accordance with Federal regulations and sponsoring agency’s policies. •Ensured proper reconciliation of AEs. •Coordinated study initiation and closeout procedures. • Scientific writing of protocols, consent forms, abstracts and articles. •Reviewed Medical Charts. Show less

• Research thesis: Friedreich’s Ataxia (FRDA) gene expression in Cellular and Animal Model & Therapeutic Essay Development.• Techniques: Cell and Molecular Biology, Experimental Pharmacology