Capabilities

What We Bring to a Study.

Mesa Clinical Research runs studies inside a working Arizona practice. That puts real patients, an experienced clinical team, and the day-to-day discipline a study depends on in one place.

Patient Recruitment

Reaching the Right Patients.

The hardest part of most studies is finding the right people in time. A working practice starts that search from people it already knows.

Patients already in care

Enrollment can begin with people the practice already treats for the condition under study.

Physician referrals

Referrals from nearby Arizona practices, built on relationships rather than cold outreach.

Local and digital outreach

Targeted advertising and community outreach across the Mesa area for studies that are open.

Reminders and follow-up

Appointment reminders and coordinator support help participants stay on schedule through the study.

Areas We Study

Adult conditions seen in everyday primary care.

Our investigators are practicing primary care physicians, so studies focus on adult conditions they manage day to day. Specific areas are confirmed as studies are awarded.

Internal medicineFamily medicineType 2 diabetesHigh blood pressureHigh cholesterolMetabolic healthVaccinesRespiratory health
Confirm the final list of therapeutic areas before publishing. These are primary care examples, not a claim of active studies in each area.

Patient Experience

Built to Be Easy to Take Part In.

Clear, unhurried consent

The study is explained in plain language, questions are welcome, and you can take the information home before deciding.

Flexible scheduling

Visits are arranged around real life wherever the protocol allows, so taking part fits alongside work and family.

A consistent point of contact

A coordinator stays with you through the study, so you always have someone who knows your situation.

A familiar local clinic

Visits happen at a clinic in Mesa, close to home, not at an unfamiliar research center across town.

No cost to take part

Study visits and study-related care are provided at no cost to participants.

Care that stays connected

With your permission, the team keeps your own doctor informed, so everyone caring for you stays on the same page.

How We Work

Standards Behind Every Study.

Good Clinical Practice

Investigators and research staff are trained to Good Clinical Practice (GCP) standards, the international benchmark for running trials ethically and reliably.

Delegation and training on file

Every study task is delegated in writing, and each team member is trained on the protocol before the first visit.

Monitor-ready data

Source documentation and electronic data capture are kept current, so the record is ready when a monitor visits.

Four clinical research colleagues talking together in a clinic office.

Work With Us

Work With Us.

We work with physicians across Arizona who want to offer their patients access to clinical trials, and with research staff looking for their next site. Tell us which you are and we will follow up.

Illustrative photograph

For physicians

Whether you want to serve as an investigator or refer patients into studies we are running, the first step is the same. A short call about the conditions you treat and the volume you see.

For research staff

Coordinators, site managers, nurses, and regulatory staff. We keep applications on file and reach out when a role opens rather than starting a search from scratch.

Specialties We Work With

Internal MedicineFamily MedicineEndocrinology and DiabetesCardiologyNephrologyRheumatologyGastroenterologyPulmonologyNeurologyPsychiatry and Behavioral HealthDermatologyWomen's Health

Adult patients only. We do not conduct oncology, pediatric, or veterinary research.

01

A conversation

We go through the conditions you treat most, your patient volume, and whether anything currently enrolling lines up.

02

Qualification

Physicians serving as investigators complete Good Clinical Practice (GCP) training and are qualified by the sponsor. Every study is reviewed and approved by an Institutional Review Board (IRB) before enrollment opens.

03

Studies run at our site

Your patients are screened, consented, and seen here. Their primary care stays with you, and you receive updates throughout, subject to their authorization.

Study placement is decided by sponsors. Investigator roles carry qualification requirements set by each protocol.

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