I'm interested in joining a study
Learn what participation involves, review currently enrolling studies, and see whether pre-screening makes sense for you.
Explore studiesClinical research site
Advancing research, with people at the center
We conduct industry-sponsored clinical trials with regulatory rigor and a bilingual team that treats every participant like a neighbor, not a number.
Where would you like to start?
I'm a sponsor or CRO
Review our site capabilities, therapeutic experience, staffing, and quality systems for protocol placement.
Site capabilitiesI'm a physician
Refer a patient to a trial, or explore sub-investigator and collaboration opportunities with our research team.
Referral informationWhat we do
Salud Clinical Services is a dedicated research site. Our team runs clinical trials on behalf of sponsors and contract research organizations, following the study protocol, applicable FDA regulations, and Good Clinical Practice guidelines.
We are not a treatment clinic. Everything we do is research, conducted under the oversight of an Institutional Review Board that reviews each protocol before a single participant is enrolled.
- Bilingual English/Spanish research staff
- Experienced Principal Investigators and coordinators
- IRB-reviewed protocols and documented staff training
- HIPAA-aligned handling of participant information
Why participation matters
Every approved medication available today exists because volunteers took part in research. Participation is always voluntary, always explained in advance, and can be stopped at any time without affecting the care you receive elsewhere.
View all enrolling studies
Studies open and close over time. The enrolling studies page always reflects what is currently available at our site.
Frequently asked questions
Answers to questions we hear most often.
What is Salud Clinical Services?
We are a clinical research site. We conduct clinical trials sponsored by pharmaceutical companies and research organizations. We do not provide routine or ongoing medical care.
Does it cost anything to participate in a study?
Study-related visits, assessments, and investigational product are provided at no cost to participants. The informed consent document for each study explains exactly what is and is not covered.
Do I need health insurance to take part?
Insurance is generally not required for study-related visits. Requirements can vary by protocol, and the study team will review the specifics with you before you decide.
Do you have Spanish-speaking staff?
Yes. Our team is bilingual, and consent materials for our studies are available in English and Spanish.
How do I know if I qualify for a study?
Each study has eligibility criteria defined by its protocol. A short pre-screening conversation with our coordinators is the first step; final eligibility is confirmed at a screening visit.
Have a question about clinical research?
Our coordinators can walk you through what participation involves, with no obligation to enroll.
Contact our team