At SitePath Clinical Research, our investigators and physicians are recognized leaders in their respective specialties. United by a shared commitment, they advance clinical science, improve patient outcomes, and foster innovation through collaboration and clinical excellence.
Redefining Access and Excellence in Clinical Research
SitePath Clinical Research is a dynamic and growing network of fully integrated clinical research sites across the United States. Our mission is to conduct high-quality, compliant clinical trials while expanding access for underserved and diverse communities. We are dedicated to empowering emerging investigators and fostering inclusive research environments that drive meaningful change in healthcare.
As demand for qualified principal investigators rises, SitePath Clinical Research addresses this need by mentoring and supporting new sub-investigators and principal investigators through expert training and continuous guidance. Our experienced leadership team has a proven track record of building high-performing research sites, developing future investigators, and establishing lasting partnerships with sponsors, CROs, academic institutions, and community-based organizations.
At SitePath, we believe clinical research should be accessible, inclusive, and impactful. Through our collaborative, physician-led model, we deliver results that advance science and improve patient care.
At SitePath Clinical Research, we help physicians integrate seamlessly into the field of clinical research. Our structured, step-by-step model supports your progression—from introducing research into your practice to leading studies as a principal investigator.
Start by integrating clinical research into your current medical practice. This early-stage collaboration allows you to offer patients access to novel care options—while preserving your trusted physician-patient relationship. Once you express interest, our Regulatory Team will walk you through study protocols, eligibility criteria, timelines, and patient benefits, including advanced screenings and innovative therapies.
This step is ideal for physicians looking to expand their services and provide patients with access to cutting-edge clinical opportunities.
As a sub-investigator, you will participate in clinical trials under the guidance of an experienced principal investigator. SitePath Clinical Research provides comprehensive training in research ethics, study conduct, regulatory compliance, and documentation standards.
Each study is matched to your clinical specialty and patient population, allowing you to gain hands-on research experience while continuing to provide high-quality care. Our mentorship model supports your professional development and ensures compliance at every step.
With growing experience and guided mentorship, you’ll be well-prepared to assume the role of Principal Investigator. SitePath Clinical Research supports your credentialing with sponsors and CROs, helping you secure leadership roles in upcoming trials.
As a PI, you will oversee study conduct, ensure patient safety, and uphold data quality standards. Compensation is aligned with your responsibilities, leadership, and time commitment. Throughout your journey, our team provides comprehensive operational, regulatory, and logistical support—so you can stay focused on what matters most: advancing clinical research and improving patient outcomes.
Ensuring Compliance Every Step of the Way
SitePath Clinical Research provides comprehensive regulatory and operational support from study startup to closeout. Our expert team ensures adherence to all applicable guidelines, helping investigators navigate protocol requirements, documentation, and site audits with confidence and ease.
Streamlining Research with Smart Solutions
SitePath equips investigators with advanced digital tools—including CTMS platforms, eRegulatory systems, and real-time reporting dashboards—to optimize workflows, ensure compliance, and enhance productivity across every stage of the clinical trial process.
Equipping You with Tools for Success
SitePath Clinical Research offers comprehensive, hands-on training in GCP compliance, research conduct, and site operations. Our tailored recruitment strategies are designed to match your patient population and therapeutic focus—ensuring strong enrollment, retention, and trial performance from the start.
Focused on Your Success
At SitePath Clinical Research, we prioritize your role as a physician and investigator. Our comprehensive support model allows you to concentrate on what matters most—providing exceptional patient care while leading high-impact clinical research with confidence.
At SitePath Clinical Research, we support you at every stage of the research journey. Our team provides clear, objective education on the clinical trial process—empowering you to make informed decisions for your practice and your patients.
We uphold the highest standards of ethics and compliance, prioritizing patient safety while ensuring scientific rigor. With SitePath, you can move forward with confidence—knowing your research is built on transparency, trust, and excellence.
Investigators and Physicians, complete the form to collaborate and advance medical innovation!
