For sponsors and CROs
One team, every site
Symphony Research is a clinical research site network. We are not a CRO and we do not compete with yours. We are the sites that enroll, treat, and retain your patients, with one operations team and one quality standard across every location.
Centralized operations means the regulatory package, the training, the source documentation practices, and the coordinator playbook are the same in Jacksonville as they are in Philadelphia. It means one contract, one point of contact, and one answer when you ask how a study is doing.
Therapeutic experience
Wound care is our core. We have run studies in diabetic foot ulcers, venous leg ulcers, and other chronic and surgical wounds, with investigators drawn from wound care, podiatry, vascular, and primary care practices.
We also conduct studies outside wound care where our sites and investigator relationships fit, including infant nutrition, bone health, dermatology, and general medicine. If you have a protocol in an adjacent area, ask. We will give you an honest answer on feasibility.
Since 2023 we have conducted more than 18 studies across our sites.
Capabilities
- Dedicated clinical research coordinators at every site, employed by Symphony, not the practice.
- Physician investigators with direct patient relationships, supported by our oversight model.
- CTMS: CRIO. eSource and eRegulatory: Florence. EDC experience across Medidata and sponsor-specified platforms.
- Central IRB experience with Advarra and WCG.
- Participant payments through ClinCard.
- Recruitment: targeted local outreach run by our team for each study, in addition to investigator practice populations.
- Retention: coordinator-managed scheduling and Symphony-funded door-to-door transportation for participants who need it.
- Rapid startup. Regulatory, contracting, and training run in parallel from a standing template.
Patient access
Our investigators are practicing physicians, so our patient access is their active patient panels plus the new patients our outreach brings in for each study. Ask us for current volume by indication and site as part of feasibility.
Sites
Headquarters in Jacksonville, FL, with research sites in Jacksonville and Jacksonville Beach, FL, and Philadelphia, PA. Full addresses are on our Locations page.
Start a feasibility conversation
Send us the indication and a summary of the protocol, or the feasibility questionnaire itself, and we will respond within two business days with a candid assessment.