Clinical Research in Portland, OR

Northwest Research is a medical research organization located in southeast Portland, Oregon. We connect people with opportunities to advance healthcare forward through the development of safe, reliable, and effective medications, devices, and treatment regimens. Our mission is to provide meaningful data for the advancement of medical care. We are also dedicated to bringing earth-friendly medicines to the market.

What is Clinical Research?

Clinical research helps doctors and other healthcare providers learn new ways to prevent and treat illness in people and find answers to questions about health, disease, and human behavior. Clinical research leads to the development of new drugs, new ways to treat old and new illnesses, and new ways to prevent diseases in people at risk of developing them.

How Clinical Research Works

Discovery and Pre-clinical Trials

Long before reaching the clinical trial phase, researchers test and discover new medications and medical treatment regimens in a lab. If a treatment seems promising, it undergoes rigorous testing to evaluate its effectiveness, appropriate dosage, if it interacts with other drugs, and more. Then, the treatment moves to the pre-clinical trial phase where it is determined whether or not the treatment is safe for human testing. For a treatment to reach the clinical trial phase, it must meet a set of robust safety and effectiveness guidelines.

Clinical Trial Design

Researchers design a detailed plan for conducting clinical trials, called a protocol. The protocol is like a roadmap to the study and helps dictate who qualifies to participate in the study, how long it will last, how data will be collected and analyzed, and more. Clinical trials must meet federal standards and receive approval from the Food and Drug Administration (FDA) before moving forward.

Every clinical trial has a Sponsor who oversees the process. This includes identifying an appropriate sites where the trial will take place. A host site is responsible for coordinating the study, finding volunteers to participate, implementing the study protocol, and more.

Clinical Trials

Clinical trials have a set of guidelines that dictate who is eligible for participation. The facility conducting the study seeks out volunteers who meet these guidelines. The facility conducts a detailed informed consent process with prospective participants, ensuring that volunteers understand each step of the protocol and what the clinical trial entails.

When a volunteer officially consents to participate in a study, they will receive research-related care, evaluations, and supervision through the facility conducting the study. The facility works closely with the Sponsor and an Institutional Review Board (IRB) to ensure both the protocol and all federal regulations are closely followed.

Areas of Study

  • Chronic Cough

  • COPD

  • Seasonal & Chronic Allergies

  • Skin Conditions

  • Asthma

  • Diabetes

  • Weight Management

  • Sleep Apnea

  • Non-Allergic Rhinitis

  • Viral Infection

Why participate in clinical research at Northwest Research Center?

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Meet our team

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Anthony Montanaro, MD

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Subra Seetharaman, MD, FAPCR

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Carol Pehl, RN, CCRC

Site Manager

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Danielle Law

Team Leader

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Jade Fairchild, CCRC

Study Coordinator

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Barry Rhodes, MD

Investigator

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Melissa Bonilla, CRC

Study Coordinator

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Lisa Zeigler, CRC

Study Coordinator

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Brittany V, MPH, CRC

Study Coordinator

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Andrzej Stadnik, PA-C, MPH

Investigator

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Rebecca Raccanelli

Study Coordinator