For physicians

You see the patients. Some of them have a wound that will not close, a condition that standard care has stopped helping, or no good option left on the table. A clinical study can be that option. The obstacle has always been that running one takes a coordinator, a regulatory binder, a monitor visit schedule, and a dozen other things a practice does not have room for.

That is the part we do. Symphony Research places a study in your practice and staffs it. You serve as the principal investigator and see your patients the way you already do. Our coordinators handle everything else.

1. We qualify the fit. A short conversation about your patient population and the studies we have open. If there is a match, we move forward. If not, we tell you.
2. We set up the study. Regulatory submissions, IRB approval, sponsor contracting, training, and supplies. Your involvement is a few hours of onboarding and the investigator training the protocol requires.
3. We run it in your office. A Symphony coordinator is on site for study visits, manages scheduling and documentation, and is your single point of contact. You provide the clinical oversight and care.

Study-related visits, exams, and the investigational treatment at no cost to them or their insurance. Compensation for their time on most studies. Door-to-door transportation when they need it. And a study team that knows them by name and stays with them from the first visit to the last.

• Investigator fees, paid per visit plus a monthly amount, set study by study.
• No new staff, no new overhead, no new software. We bring the coordinator, the systems, and the supplies.
• New patients. We run targeted local outreach for each study, and those patients come to your practice.
• Retention. Patients in a study see you more often and stay with the practice.
• Experience as a principal investigator on sponsored research, which is its own credential.