The Trialogic Site Management group is comprised of private physician practices, clinics, and hospitals that conduct clinical trials.  Each of our facilities are staffed with dedicated clinical research personnel that work within a structured team environment.  Each trial is assigned to a study team consisting of a Principal Investigator, Sub-Investigator(s), Study Manager and Study Coordinator(s).  The Study Manager plays the role of an auditor/trainer to ensure that our operations maintain balance between good clinical practices, protocol directives and our internal SOPs, which are firmly based on the FDA code of federal regulations.  Our systematic reporting and accountability structure provides a strong foundation for consistent compliance.

Our Standard Operational Procedures are reviewed for revision twice yearly as we understand that the research process must adapt to the constantly changing needs of the patients that we serve.  Regulatory documents, IRB submissions and contractual agreements are typically completed and turned around within 5 business days.  Our primary focus is patient safety and data quality.  With that said, we consistently meet or exceed our enrollment goals.  Trialogic facilitates trials for multiple therapeutic areas including but not limited to the following:

• Allergy/Immunology
• Alzheimer’s
• Cardiovascular Diseases
• CNS
• Depression
• Family Practice
• Gastroenterology
• Geriatric Medicine
• Hematology
• Internal Medicine
• Infectious Diseases
• Nephrology
• Oncology
• Ophthalmology
• Pain
• Podiatry
• Pulmonary Disease
• Rheumatology
• Surgery (Various)
• Sickle Cell Anemia
• Urology
• Women’s Health

The number of investigators and therapeutic areas served are constantly growing.