lwanga karoli

Research assistant at Kenya Medical Research Institute/Centre for Global Health Research (KEMRI/CGHR)

since October, 2022

ka***a0@gmail.com

Work experience

i.Develop an in-depth understanding of the study’s goals and activities to conduct the study
ii. Perform screening & consenting, enrollment, prescription of medications and follow up of participants, including medical history, physical examination and
iii. Document applicable study data during all study procedures
iv. Clinical management of ill participants and conducting clinical procedures including venipuncture, insertion of IV cannulas and collection of biological samples when necessary
v. Report any adverse events to the Study Pediatrician, PI, MO and Study Coordinator
vi. Ensure that all the necessary documentation pertaining to screening, enrollment, follow up, clinical processes, other specific study procedures and operations are documented in the proper manner as provided for and in conformity with good clinical and documentation practice
vii. Respond to and resolve queries about participants’ information documented in the study files
viii. Adequately respond to questions about the study posed by participants and the community ix. Offer basic nursing care to the study participants
x. Make diagnoses and decisions on patient’s management according to study protocols and the recommended national guidelines
xi. Arrange laboratory tests according to study protocol
xii. Any other duties as assigned by the immediate supervisor