Cardiologist & Investigator
Haris Turalic, MD
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.
Profile
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.
- Profile
- Cardiology
- At Salud since
- 2025
- Languages
- English and Spanish
Education and training
- Cardiology Fellowship — North Shore/LIJ Health System (Northwell, Hofstra School of Medicine), Manhasset, NY, 2007–2010
- Cardiology Fellowship — New York University Medical Center, New York, NY, 2004–2007
- Doctor of Medicine — Albert Einstein College of Medicine, Bronx, NY, 2000–2004
- B.S. Biology — Brooklyn College, Brooklyn, NY, 1996–1999
Licenses and certifications
- Clinical Research — GCP certified
- Cardiac CTA — Level III
- Echocardiography — Level II
- Nuclear cardiology — Level II
- Transesophageal echocardiography
- Medical licensure: Florida, New York, Virginia, Illinois, Georgia, Kentucky
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.
Information on this website is provided for general educational purposes about clinical research and is not medical advice. Participation in any study is voluntary.