Bridging Science and Care

Our SMO model centers on deploying highly skilled Clinical Research Coordinators (CRCs) who work closely with site teams to oversee protocol compliance, documentation, and patient management.

Whether embedded within leading university hospitals or private clinical sites, our CRCs integrate smoothly into your study environment to maintain consistency and performance

Who We Help

We support every stakeholder in the clinical ecosystem:
🧪 Sponsors – faster site activation and oversight
🔬 CROs – transparent collaboration and real-time access
🏥 Sites – training, compliance, and workflow tools
👩‍⚕️ Patients – safe and supportive participation

As a vital partner to CROs, pharmaceutical companies, biotech innovators, and medical device sponsors, MedPath’s SMO services are designed to:

A Full Spectrum of Site Management Services

Identify and activate research-ready sites that match protocol requirements and patient population needs

Manage site-level operations, including logistics, documentation, and quality control

Place trained CRCs and study nurses to support daily trial activities and reduce investigator burden

Update and complete SOP according to policy and regulation

Coordinate investigator training, data entry oversight, and site audits to maintain GCP standards

Support patient recruitment and retention with strategies tailored to the Study

Partner with MedPath and discover a smarter, stronger approach to clinical site management.

Choosing MedPath as your SMO partner means gaining a responsive, experienced team committed to operational excellence. Our deep understanding of the clinical research environment—paired with our hands-on support—ensures that your clinical trial not only stays on track, but exceeds expectations