- acilitated efficient organization of study-related documents through meticulous record-keeping practices.
- Educated patients regarding all facets of clinical study participation.
- Assisted with research protocol development.
- Coordinated with multidisciplinary teams to facilitate smooth communication between researchers, clinicians, and support staff.
- Streamlined data collection processes for improved accuracy and efficiency in clinical research projects.
- Demonstrated advanced knowledge of federal regulatory compliance guidelines.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Managed patient recruitment, informed consent process and data entry to support trial objectives.
- Research Experience at Jordan Hospital (two studies and one database collection for a group of cardiology studies):
1. Prevalance of Nosocomial Clostridium difficile Infections in Amman, Jordan: A Multicenter Study (Ongoing Study).
2. Prevalance and Antimicrobial Susceptibilities of Microorganisms Causing CVC infections and CLABSI in Pediatric Patients (Ongoing Study).
*Both studies were conducted by Dr. Jamal Al-Wadi (ID Consultant – Jordan Hospital)*
3. Database collection for The First Registry in Jordan (JoPCRI).
- Collaborated with interdisciplinary healthcare teams for optimal patient care and improved treatment outcomes.
- Developed strong relationships with healthcare providers, facilitating communication and collaboration for better patient care coordination.
- Educated patients on proper medication use and adherence, leading to improved health outcomes and decreased hospital readmissions.
- Evaluated medication regimens for complex patients, identifying potential drug interactions and devising alternative treatment strategies when necessary.