Boeson Research capabilities overview
Independent, multispecialty clinical research in Montana and Utah.
Locations
Research
Boeson conducts Phase II–IV drug trials and other clinical and observational research, including device and specimen-collection studies. Research interests and experience described by our team include women’s health, pediatrics, vaccines, internal medicine, diabetes, mental health, immunology, pain, and devices. Specific investigator and site capabilities are confirmed during feasibility.
Research systems
Boeson uses RealTime CTMS and electronic research records. Research submissions are handled through designated research systems, separately from general website contact messages. Protocol-specific workflows, access, and data requirements are discussed during startup.
Pre-screening
Boeson’s Master Pre-Screening and Screening Plausibility Protocol, BR-REC-001 Version 1.1 dated September 14, 2026, was approved by Pearl IRB under IRB ID 2026-0457. This framework supports permission-based preliminary assessment. It does not establish trial eligibility, replace study-specific consent, or approve unrelated recruitment materials.
Select the right combination of investigators and sites
Use Boeson’s complementary specialties to build a stronger shortlist. Request an assessment of one location, compare two or more sites for the same protocol, or identify investigator teams for multiple studies in your program.
Explore multi-site selection opportunities
Investigator and location capabilities
Missoula
Maternal-fetal medicine, obesity and metabolic research, cardiology, dermatology, nephrology and neuropsychology, with additional podiatric research experience.
Great Falls
OB/GYN and reproductive-health research, vaccines and rheumatology, supported by internal-medicine Sub-I experience.
Bozeman
Vaccine and infectious-disease expertise through the Bozeman Health collaboration and Dr. David Taylor’s extensive clinical-development background.
Provo and Salt Lake City
Provo combines psychiatric research with cardiovascular and lipid expertise, and adds ENT clinical expertise through Dr. Seth Riddle, who is new to Boeson. Salt Lake City adds adult and geriatric psychiatric experience. Investigator availability and procedures are evaluated by location.
From protocol review to startup
- Assess clinical fit: Match the population and procedures to the investigator’s qualifications and relevant research history.
- Assess delivery: Review staffing, visits, recruitment sources, equipment and any external facility arrangements.
- Plan startup: Identify the required documents, study training, budget, contract and activation dependencies.
- Agree on study workflows: Establish source-record, data-entry, monitoring-access and communication requirements for the protocol.
What to share for a useful feasibility assessment
Send a nonconfidential synopsis with the indication, age range, key eligibility criteria, proposed procedures, target enrollment, visit schedule and anticipated startup window. Flag unusual equipment, imaging, specimen-processing or safety requirements early.
Request investigator CVs, relevant study experience and a site-by-site feasibility response. Compare recruitment plans, procedure delivery and startup requirements before selecting your Boeson sites.
Explore therapeutic expertise · Review investigator backgrounds
Feasibility discussion
Share a nonconfidential outline of your study, the population, proposed locations, key procedures, and expected timeline. We can then discuss the relevant investigator, staffing, facility, and operational requirements.
Next steps
Discuss Feasibility · Meet Our Investigators · View Locations
Reviewed September 16, 2026. Use your browser’s Print command for a clean copy.