FIDES Clinical Research About Us
About FIDES Clinical Research

Committed to Better Outcomes

At Fides Clinical Research, our mission is to advance the future of medical care by conducting ethical, high-quality clinical research that provides patients with access to innovative therapies.

We are committed to scientific excellence, patient safety, regulatory compliance, and meaningful collaboration with partners, CROs, and healthcare providers.

Through compassionate care and rigorous research practices, we strive to improve treatment options and outcomes for individuals living with chronic disease.

Our Purpose

To improve lives by advancing scientific research and delivering new treatment options for patients in need.

Patient Focused

Putting patients at the center of everything we do.

Science Driven

Advancing medical care through innovative research.

Better Tomorrow

Working today for healthier, stronger communities.

Compassionate Care

Every patient. Every step. Every time.

Our Purpose

Improving Lives Through Research, Experience, and Community

Our Mission

To conduct high-quality clinical trials that advance medical science and provide patients with access to innovative therapies.

Our Experience

Our team brings extensive experience in clinical research, regulatory compliance, patient care, and chronic disease research.

Our Community

We believe in building strong relationships with patients, partners, healthcare providers, and communities.

Meet Our Team

Our Clinical Research Leadership

Principal Investigators

Dr. Elizabeth Nguyen

Dr. Elizabeth Nguyen, MD

MD Principal Investigator

Dr. Elizabeth Nguyen, MD, is a board-certified Nephrologist with more than 20 years of clinical experience. She brings deep expertise, strong clinical judgment, and a long history of patient-centered care to her role as Principal Investigator.

  • Board-Certified Nephrologist
  • 20+ years of clinical experience in nephrology and internal medicine
  • Active clinical practice at Northside Hospital, Sandy Springs
  • Deep experience in CKD, ESRD, dialysis, and renal therapeutics
  • Strong commitment to patient safety, ethics, and protocol compliance
Education and Professional Background
Medical School
The University of New South Wales.
Kensington. N.S.W, Australia
Residency
The Good Samaritan Hospital, affiliated with The Johns Hopkins Hospital, Baltimore, MD
Nephrology Fellowship
Tulane Hospital. New Orleans. LA
Hospital Affiliation
Northside Atlanta Hospital
Emory Saint Joseph's Hospital
Board Certification
ABIM certified in Nephrology

Dr. Elizabeth Nguyen, MD joined North Atlanta Kidney Specialists in 2005. She is the Medical Director of DaVita North Fulton, DaVita Lake Hearne and DaVita Home Training of North Atlanta. Her clinical area of interest include peritoneal dialysis and hypertension.

She has been the recipient of several nephrology awards including the Castle Connolly Top Doctor award since 2017 featured in the Atlanta Magazine in 2018, 2019, 2020, 2021 and Modern Luxury - The Atlanta Magazine in 2022, 2023.

Sub-Investigator

Carden Safran Toti

Carden Safran Toti

MSN, APRN Sub-Investigator and Infusion Nurse Specialist

A board-certified nurse practitioner, Carden completed her bachelor’s degree at the University of Chicago. She studied nursing at NYU and obtained her master’s in nursing science at Emory University, graduating with specialty degrees in adult- gerontological primary care and women’s health.

She was awarded the honor of membership in the Sigma Theta Tau International Honor Society of Nursing at both Emory and NYU.

Research Team

Our research team is committed to advancing clinical research through collaboration, integrity, and excellence. Together, they support high-quality studies, efficient site operations, and a positive experience for patients and research partners.

FIDES Clinical Research Team workspace

Sofia Shamim

Lead Clinical Research Coordinator ECFMG Certified, International Medical Graduate

She is responsible for overseeing site selection visits, study start-up activities, and overall clinical trial operations. Manages regulatory and IRB submissions, essential regulatory documentation, compliance requirements, and maintenance of investigator site files. Provides comprehensive study management and coordination throughout the study lifecycle while ensuring adherence to protocols, ICH-GCP, and applicable regulations. Oversees development, implementation, and maintenance of SOPs to ensure consistent, compliant, and efficient site operations.

Together, We Are Building a Healthier Future

Through collaboration, innovation, and compassion, FIDES Clinical Research is committed to making a meaningful difference in the lives of patients.