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Our team

Investigators and research staff

Experienced clinicians and coordinators who guide every protocol from feasibility through close-out.

How our team is organized

Every study is led by a Principal Investigator who holds ultimate responsibility for participant safety and protocol conduct. Coordinators manage visits and source documentation, and a regulatory manager maintains essential documents and IRB correspondence.

Frequently asked questions

Answers to questions we hear most often.

What is a Principal Investigator?

The Principal Investigator is the qualified clinician responsible for conducting the study at the site, protecting participant safety, and ensuring the protocol is followed.

Who will I see at my study visits?

Most visits are conducted by a clinical research coordinator, with the Principal Investigator or a sub-investigator involved in medical assessments and safety review.

Is the research staff trained in Good Clinical Practice?

Yes. GCP and protocol-specific training is completed and documented before staff are delegated study responsibilities.

Can I request a Spanish-speaking coordinator?

Yes. Our team is bilingual and visits can be conducted in English or Spanish.

Questions for our research team?

Reach out and we will connect you with the right person.

Contact us

Information on this website is provided for general educational purposes about clinical research and is not medical advice. Participation in any study is voluntary.