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Our team

Investigators and research staff

Experienced clinicians and coordinators who guide every protocol from feasibility through close-out.

Mayelin Amoros Duquesne, MD, MHA

Mayelin Amoros Duquesne, MD, MHA

Principal Investigator — Internal Medicine

Dr. Mayelin Amoros is a board-certified Internal Medicine physician with experience in Phase II–IV clinical trials and a versatile practice encompassing primary care, hospital medicine, and hospice care. Her involvement across multiple levels of patient care gives her a comprehensive perspective on acute, chronic, and complex medical conditions. Fluent in English and Spanish, Dr. Amoros brings a patient-centered approach and a strong commitment to advancing clinical research.

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Haris Turalic, MD

Cardiologist & Investigator

Dr. Haris Turalic is an experienced cardiologist and clinical investigator with expertise in cardiovascular medicine, advanced cardiac imaging, and the management of complex cardiac conditions. His active cardiology practice and extensive diagnostic capabilities provide a strong clinical foundation for cardiovascular research and access to a broad patient population. GCP-certified, Dr. Turalic combines clinical expertise, research experience, and physician leadership to support high-quality clinical trial execution.

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Danay Suarez Falcon, MD

Danay Suarez Falcon, MD

Sub-Investigator — Internal Medicine

Dr. Danay Suarez Falcon is a board-certified Internal Medicine physician whose practice integrates primary care, hospital medicine, and hospice care with experience in Phase II–III clinical research. Her hands-on clinical work with medically diverse patients supports a practical, real-world approach to research and patient recruitment. Fluent in English and Spanish, Dr. Suarez is dedicated to delivering high-quality patient care while contributing to meaningful clinical research.

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How our team is organized

Every study is led by a Principal Investigator who holds ultimate responsibility for participant safety and protocol conduct. Coordinators manage visits and source documentation, and a regulatory manager maintains essential documents and IRB correspondence.

Frequently asked questions

Answers to questions we hear most often.

What is a Principal Investigator?

The Principal Investigator is the qualified clinician responsible for conducting the study at the site, protecting participant safety, and ensuring the protocol is followed.

Who will I see at my study visits?

Most visits are conducted by a clinical research coordinator, with the Principal Investigator or a sub-investigator involved in medical assessments and safety review.

Is the research staff trained in Good Clinical Practice?

Yes. GCP and protocol-specific training is completed and documented before staff are delegated study responsibilities.

Can I request a Spanish-speaking coordinator?

Yes. Our team is bilingual and visits can be conducted in English or Spanish.

Questions for our research team?

Reach out and we will connect you with the right person.

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Information on this website is provided for general educational purposes about clinical research and is not medical advice. Participation in any study is voluntary.