Who We Are


SMO-USA, Inc. was created in 1997, and has conducted over 1,000 different clinical trials since then. Our network of highly qualified, capable, and enthusiastic Investigators now number in excess of 3,500 physicians representing most therapeutic specialties.  It is not just the strength and commitment of our Investigators that is the foundation of our success, but the experience and dedication of the Clinical Research Coordinators assisting these physicians in the preparation and conducting of these trials.

Our business practices are consistent with the Code Of Ethics promoted by the Association of Clinical Research Professionals.

What We Do

We present qualified, pre-screened, Principal Investigators for participation in clinical trials in most therapeutic specialties. We have developed effective and stable relationships with many highly experienced, qualified and enthusiastic Clinical Investigators and Clinical Research Coordinators throughout the United States. This includes single practitioners, large single and multi-specialty practices, physician networks, hospital based physician's, and academic medical centers. All of the Investigators within the SMO-USA, Inc. network have been evaluated to ensure they not only are qualified to conduct clinical trials and understand regulations regarding the conducting of clinical trials, but have the patient population and administrative capabilities to properly conduct them. They must meet specific minimal standards before being included in the network.  We only present those Investigators meeting the specific selection criteria outlined by the Sponsor or CRO. This eliminates a significant amount of time and expense when attempting to qualify, enroll, and initiate a site.

We Ensure Timely and Accurate Regulatory Board Submission and Data Collection
All sites have dedicated, full time, and experienced clinical research coordinators to ensure the prioritized and accurate submission of regulatory documents, appropriate site orientation/initiation, patient recruitment, screening and enrollment as well as the collection of clean and accurate data. Our own internal management and quality assurance practices further assures that tasks are completed quickly and accurately and any problems that jeopardize the success of the study are quickly identified and resolved.

We Provide Access to Large Patient Populations
Prior to us presenting an Investigator for study participation, we assess the patient population from which study subjects will be drawn to assure the increased likelihood of enrollment goals being met. Although we believe that carefully orchestrated advertising can assist in meeting enrollment goals, we firmly believe that the site must have the patient population or internal referral base from which to enroll patients.

We Provide Effective Communication Between Sites, Investigators, and Customers
The cornerstone of any successful clinical investigation is ongoing support and communication between all parties. Because of our commitment to the successful outcome of every study in which we participate, an internal Project Manager is assigned to each study to ensure that communication is maintained and that the study receives the full attention it deserves until completion. There are numerous variables and situations that arise during the conduct of a study that could compromise it’s outcome, and this demands a professional with expertise, strong problem solving skills, and attention to detail to overcome those obstacles. We provide that experience.



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