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Hire Dr. Chaima S.
Belgium
USD 70 /hr
Clinical Research Specialist/ PhD in Molecular Biology/ Hematology / & Oncology ztrials/ Clinical Data & Protocol Mana
Profile Summary
Subject Matter Expertise
Services
Work Experience
PhD Researcher in clinical trials coordination.
CHU-Brugmann
September 2019 - Present
Study Coordinator
Centre Hospitalier Universitaire Brugmann
September 2019 - Present ![]()
Education
PhD in Biology
Faculté des sciences de Tunis
September 2010 - April 2015
PhD (Biology)
Faculty of Sciences of Tunis
September 2010 - April 2015 ![]()
Master in Genetics
Faculté des sciences de Tunis
September 2008 - September 2010
Certifications
Publications
JOURNAL ARTICLE
Dabboubi R, Amri Y, Yahyaoui S, Mahjoub R, Sahli CA, Sahli C, Hadj Fredj S, Bibi A, Sammoud A, Messaoud T (2020). A new case of congenital atransferrinemia with a novel splice site mutation: c.293-63del . European journal of medical genetics.
Laouini N, Sahli CA, Jouini L, Haloui S, Fredj SH, Daboubi R, Siala H, Ouali F, Becher M, Toumi N, et al. (2017). Determination of glucose-6-phosphate dehydrogenase cut-off values in a Tunisian population . Clinical chemistry and laboratory medicine.
Doggui R, Abdelhafidh Sahli C, Aissa WL, Hammami M, Ben Sedrine M, Mahjoub R, Zouaoui K, Daboubi R, Siala H, Messaoud T, et al. (2017). Capillarys 2 Flex Piercing: Analytical performance assessment according to CLSI protocols for HbA<sub>1c</sub> quantification . Electrophoresis.
Sahli CA, Ben Salem I, Jouini L, Laouini N, Dabboubi R, Hadj Fredj S, Siala H, Othmeni R, Dakhlaoui B, Fattoum S, et al. (2016). Setup of a Protocol of Molecular Diagnosis of β-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC) . Journal of clinical laboratory analysis.
Haloui S, Laouini N, Sahli CA, Daboubi R, Becher M, Jouini L, Kazdaghli K, Tinsa F, Cherif S, Khemiri M, et al. (2016). Molecular identification of Gd A- and Gd B- G6PD deficient variants by ARMS-PCR in a Tunisian population . Annales de biologie clinique.
Sahli CA, Gritli S, Dabboubi R, Omar S, Siala H, Kaabachi N, Bibi A, Messaoud T (2015). Fortuitous description of haemoglobin A2' [δ16 (A13) Gly→Arg (GGC→CGC)] in a Tunisian family: study of the molecular defect and its origin . Annales de biologie clinique.
Sahli CA, Bibi A, Ouali F, Fredj SH, Dakhlaoui B, Othmani R, Laouini N, Jouini L, Ouenniche F, Siala H, et al. (2013). Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia . Clinical chemistry and laboratory medicine.
Sahli CA, Bibi A, Ouali F, Siala H, Fredj SH, Othmani R, Ouenniche F, Cheour M, Fitouri Z, Becher SB, et al. (2012). δ0-Thalassemia in cis of βKnossos globin gene: first homozygous description in thalassemia intermedia Libyans and first combination with codon 39 (C→T) in thalassemia intermedia Tunisian patients . Clinical chemistry and laboratory medicine.
Bibi A, Jouini L, Sahli CA, Hadj Fredj S, Abidi K, Gharsallah L, Mathlouthi S, Ouali F, Siala H, Belhaj R, et al. (2012). Detection of a novel splicing mutation causing analbuminemia in a Libyan family . Clinical biochemistry.
Bibi A, Touhemi I, Sahli C, Siala H, Bartagi Z, Koubaa D, Le Gallais D, Fattoum S, Messaoud T (2012). Fortuitous description of hemoglobin Hope in a high-level Tunisian athlete: molecular diagnosis and origin . Annales de biologie clinique.