Dr. Ibrahim Amjad​ MBA FACS FAAP


   Tel +1 (305)2678885

​​​Clinical Research Coordinator (CRC)

Xoana Zampieri, RN, BSN, WCC, CPN, CWOCN is a graduate from Barry University and registered nurse since 2006. Has been wound care certified since 2008 with widespread experience with adults and pediatrics. She has done extensive evidenced based literature research to develop policies, protocols and guidelines to standardize and improve patient care. Xoana has completed the Good Clinical Practice Certification and is working towards achieving her clinical research coordinator certification (CCRC).


Principal Investigator (PI)

Ibrahim Amjad, MD MBA, FACS, FAAP, is Board Certified in Plastic Surgery and General Surgery.  As the Assistant Professor of Plastic Surgery and having completed an AGCME approved a pediatric craniofacial fellowship, he has extensive experience in treating patients of all ages. Dr. Amjad was accepted into an accelerated BS/MD program completing his undergraduate and medical degrees in 6 years not the standard 8.  The program at Albany Medical College leads him to a General Surgery residency at Mt. Sinai- Miami Beach.  After completing a full surgical residency he continued to a plastic surgery fellowship at Summa Healthcare in Akron, Ohio.  Dr. Amjad’s furthered his training with a pediatric plastic surgery and pediatric/adult craniofacial fellowship at Miami Children’s Hospital in Miami, Florida. He is a fellow of the American College of Surgeons and a Fellow of the American Academy of Pediatrics. Dr. Amjad is a member in good standing of the American Society of Plastic Surgeons and the American Association of Pediatric Plastic Surgeons.  

Dr. Amjad is an Assistant Professor of Plastic Surgery at Florida International University.

Contact us regarding on-going research studies


Our Research Team

The Research Team will:

  • Ensuring that study data is accurately collected and reported
  • Work with the Quality Assurance Monitor and data management staff to identify and resolve data and reporting issues
  • Report and document safety issues (e.g. adverse events)
  • Participate in the preparation or review of documents exchanged with  the institutional review board (IRB)
  • Participate in protocol review or study procedures planning
  • Participate in conducting subject visits
  • Collect accurate, verifiable data, source documents, and essential documents
  • Prepare for and participate in sponsor audits and/or regulatory inspections, if applicable
  • Participate in the informed consent process