Research Project Coordinator
American University of Beirut
Total years of experience :11 years, 3 Months
Devise and structure a database to allow proper tracking and follow-up of patients.
Work with nurses, GPs, therapists to deliver healthcare services to vulnerable population and refugees.
Conduct health promotion seminars and workshops.
Enhance the total wellbeing and quality of life of refugees
Epidemiology, Biostatistics and Further Biostatistics courses.
•Attend to students’ questions and enquiries regarding the lecture.
•Lead the practical sessions at the computer lab.
•Conduct seminar sessions for article discussions.
Develop a structured database for tracking Tuberculosis (TB) cases and follow-up.
Ensure accurate and prompt collection of TB data from the different TB centers
falling under the National Tuberculosis Program (NTP) in Lebanon.
Analyse data using epidemiological methods and statistical softwares such
as Excel, SPSS and Stata.
Draft monthly reports on the numbers and distribution of tuberculosis cases across
Lebanon, disaggregated by age, gender and nationality.
Visit TB centers and act as a liaison between IOM emergency health team
and the NTP coordinator.
Participate in assessments/surveys of the beneficiaries’ health needs and needs
of the supported TB centers.
Monitor health projects’ processes to increase effectiveness.
Recommend appropriate actions in coordination with the National Public
Health Specialist and Health Programme Officer at IOM, Beirut.
Oversees and coordinates the operations of the MSc SHARP program (Scholars in HeAlth Research Program).
Coordinates activities related to the program. This includes coordinating with various institutional constituents, such as the Office of Grants and Contracts, the Research Education Unit and the Institutional Review Board.
Prepare seminars, workshops, and courses provided by the program.
Draft, edit, and submit research documents, proposals, manuscripts, etc.
Organise SHARP records and set objectives to improve efficiency of the operations within the SHARP.
Coordinate and implement a clinical trial.
Assist in the process of protocol writing, where applicable.
Schedule patient visits, maintain contact lists and patient appointments, and manage research records.
Document and edit Case Report form (CRF).
Keep accurate records of all essential study documents.
Submit progress reports to Institutional Review Board (IRB).
Prepare abstracts, posters, power point presentations and manuscripts.
Thesis submission June 2020 Thesis title: Investigating the burden of asthma co-morbidity in the UK.
Pre-medicine track