Select specialty investigators and community-based research sites across Montana and Utah. Bring us one protocol—or a program that needs more than one Boeson site.
Find investigators through therapeutic expertise
Begin with relevant clinical and research experience, then review each investigator’s published site affiliations. Operational support and investigator availability are evaluated for your protocol.

Aubrey Remmers, MD
Family medicine & obesity medicine
Obesity-medicine expertise and a broad PI portfolio spanning weight management, diabetes, cardiovascular risk and vaccines.
- Missoula · Experienced principal investigator

Jason Andersen, DO
Psychiatry
Psychiatric investigator since 2011, with adult and pediatric research experience and an interest in the psychiatric effects of GLP-1 treatments.
- Provo · Experienced principal investigator

David N. Taylor, MD, MSc
Infectious diseases, vaccines & clinical development
Board-certified infectious-disease physician and Bozeman Health Director of Clinical Research. Local PI experience includes Phase 3 influenza and RSV vaccines, Phase 2/3 therapeutics and biorepository research, backed by four decades of research leadership and former Chief Medical Officer roles.
- Bozeman · Principal investigator · Bozeman Health collaboration

M. Bardett Fausett, MD
Maternal-fetal medicine
Maternal-fetal medicine specialist with military medical leadership and research experience in maternal immunization, reproductive health and vaccines.
- Missoula · Experienced principal investigator
One program. More than one Boeson site.
Build your site shortlist around complementary investigators in Montana and Utah. Ask Boeson to evaluate two or more locations for the same protocol, or match different specialties to studies across your development program.
Women’s and maternal health
Pair Dr. Fausett’s maternal-fetal medicine expertise in Missoula with Dr. Miser’s OB/GYN research experience in Great Falls.
Vaccine programs
Review Missoula and Great Falls vaccine experience alongside Dr. Taylor’s vaccine-development leadership in Bozeman. Match investigators to the age groups and clinical demands of your program.
Psychiatric research
Evaluate Dr. Andersen in Provo and Dr. Davis in Salt Lake City for psychiatric protocols drawing on their respective research and clinical backgrounds.
Cardiovascular and metabolic programs
Connect Dr. Dahl’s cardiovascular trial leadership in Provo with Missoula’s cardiology and metabolic expertise from Dr. Jehle and Dr. Remmers.
Request a site-by-site response covering investigator fit, recruitment approach, procedures and startup needs. Each location is evaluated against your protocol, so you can select the strongest combination.
Request a multi-site feasibility review
Build your study with Boeson
Investigator and population
Match your population and protocol with relevant investigator experience and a location-specific recruitment approach.
Visit delivery
Build the visit plan around your protocol’s staffing, procedures, equipment and participant needs.
Data and oversight
We discuss source records, data-entry expectations, monitoring access, and communication responsibilities.
Startup planning
We identify document, training, budget, contract, and activation requirements.
Research systems and pre-screening
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.
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.
Start site selection with Boeson
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.
Tell us whether you are selecting one site or several. Include your key population criteria, enrollment objectives and specialized procedures so our response addresses the decisions your evaluation team needs to make.
Request a conversation
For a study application, choose your location’s RealTime listing. This form requests a reply and does not collect medical details or determine eligibility.

