
SUZAN ZIAD MAHMOUD HARB
PERSONAL DETAILS:
Date of Birth: 14/10/1982
Marital Status: single
Sex: Female.
Address: North Marka, Amman, Jordan.
Cell No. +962796274060
E-Mail: [email protected]
ACADEMIC QUALIFICATIONS:
Master’s degree in nursing management, Zarqa University in Jordan 2023.
Bachelor of Science in Nursing, Hashemite University in Jordan from 2001-2005
Scientific research published in a journals BMC nursing and Medicine journal
COMPUTER SKILLS:
Microsoft office (word, excel, PowerPoint & internet)
LANGUAGES:
Arabic and English
PROFESSIONAL EXPERIENCE
• Head of the infection control unit /Surgical Hospital from 2019 to present.
• Part time clinical instructor on Jordanian Jerman University (health assessement lab )
• Stuff Nurse in Al-Basheer Hospital ( infection control unit )2018 to 2019.
• Stuff Nurse in Al-Basheer hospital ( pediatric surgical ward) 2006 – 2018.
• Stuff Nurse Al-Mowasah Hospital 2005 – Feb 2006
• Working as a nurse (CRC) in International Pharmaceutical Research Center IPRC 2011- present
TRAINING:
• leadership on nursing
• ECG
• Deploma of clinical instructor from applied university
• Deploma of infection control from the applied university
• Deploma of risk assessement
• Training of infection control in health care USAID.
• Conferences for AMR
• Sterilization training
• Nursing process training
• TOT training
• Computer skill training
• WHONET training (AMR program from WHO)
• Conference of surgeon as speaker from 2020 till 2023.
WORKING EXPERIENCES IN IPRC:
• Responsible of all trial – related coordination decisions.
• Providing the medical care for study subjects during the whole study period.
• Develop and implement operating policies and procedures for clinical conduct.
• Reviewing and signing the clinical data as required in order to possess a thorough understanding of the medical care requirements of each study to the medical staff (Nurses and Assistant Nurses).
• Evaluation of any applicable tests during screening procedures, follow-up procedures and when required.
• Evaluation / Assessment of the study subject qualifications according to the predetermined Inclusion / Exclusion Criteria in order to obtain the medical approval on subject’s participation.
• Assessment of subject’s compliance to given treatment and reporting the adverse events , where applicable, as per the GCP, clinical protocol and IPRC general procedures.
• Perform training for the medical staff on the clinical protocol and standard procedures .
• Maintain adequate inventories of clinical supplies and materials of the clinical site in coordination with the IPRC warehouse keeper and other IPRC related departments.

