1. Curriculum Vitae
- Personal Information:
Name: Issa Ahmad Issa Ali
DOB: 16-11-1986
Nationality :Jordanian.
Marital Status:Married.
Address: Amman, Jordan.
Mobile no.: 00962 785987762/0786614803
E-mail: essaco_12@yahoo.com
‫ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــ‬
- Academic Qualifications :
• Applied Science University, BSC Nursing, June 2010.
• General secondary education certificate, scientific branch, Albaqa Secondary School,
Amman. 2004.
‫ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــ‬
- Job Experience:
1. Clinical Research Coordinator at PharmaquestJo for Drug Evaluation and Research, Amman,
Jordan Feb/2014- till now.
2. RN in the ER department at Al Istiklal hospital, Amman, Jordan. Aug/2013 Feb/2014.
3. Medical Repsentative at Al kawader Combany, Amman, Jordan Sep/2012 – Aug/2013.
4. Clinical Coordinataor at PRU, Amman, Jordan Feb/2012 – Aug/2012.
‫ـــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــ‬
I deal with so many device and equipments while we provide care such:
• Portable ECG machine.
• Suction machine.
• Dressing Set (CVP, F.Cath, Lumpur puncture,... )
• Various type of drain (chest Tube, Nasogasteric Tube, …).
• D fib
‫ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــ‬
- Languages:
Arabic: Excellent.
English: V.Good.
‫ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــ‬
- Skills :
Computer usage:
• Programs : Microsoft office skulls’ excellent.
‫ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــ‬
TRAINING:
Good Clinical Practices
Good Laboratory Practices
MAIN WORK DUTIES:
- Training clinical stuff for a new clinical study, procedure, SOPs and requirements for study.
- Preparing, design and review Standard Operating Procedure (SOP) for Clinical Department.

2. - Communicate study requirements and study progress with colleagues and management, as
well as liase with other departments.
- Prepare, review and sign-off on study specific documentation. Monitor and manage study
data in accordance to CROs Standard Operating Procedures, study protocols and pertinent
regulatory regulations and guidelines.
- Maintain close communication with principal investigator/co-investigator regarding study
progress/concerns.
- Ensure Investigator Site File is up to date.
- Assist the Clinical Data Management (CDM) in the development and review of CRFs
- Schedule and prepare for the monitoring visits & Answer study data queries.
- Document all AE’s/SAE’ S as per study requirements and act on investigator’s
recommendation for adverse event intervention.
- Maintain archive file for all completed studies recording where study files have been
stored/archived.
- Coordinate/follow up with study pharmacist to retrieve/document investigational product as
per study protocol.
- Maintain communication with the IRB regarding the following:
1.Study Progress Report
2.Safety Reports & Serious Adverse Events (SAE’ s(
- Protocol Writing, Review, Amendments & Updated Investigator Drug Brochures
- Informed Consent modifications & Administrative Changes.
- Responsible for ensuring assigned clinical trials' timelines are met.
- Maintain archive file for all completed studies recording where study files have been stored/
archived.
- Maintains a current awareness of the regulatory requirements and guidelines (FDA, EMEA,
ICH, etc…) pertaining to the conduct of clinical trials.
- Develop and maintain a working relationship with members of other departments within
CROs.
- Execute others duties as may be assigned by the Managements, update and ensure the
maintenance of clinical trial timelines.
- Carry out different medical analysis.
Reference:
- Dr. Muatasim Al-Gazawi 0777424752 Technical Manager.
- Mr. Yaheya ayassra 00962 772187070 Shift Charge.
- Mrs. Hanan Aloush 00962 795989458 Head Nurse.
- Mr. khalil aqaylah 00962 777383711 Clinical Supervisor.