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Healthy Volunteers Happy Family

Healthy Volunteers

Available for qualified participants

Healthy Volunteers

Available for qualified participants

Healthy Volunteers Happy Family

Healthy Volunteers Research Trial

CenExel CBH is conducting a clinical research study for healthy volunteers

Why participate in a clinical research study?
Clinical studies are what allow all medications and vaccines to come to market, including drugs that treat pain, infections, and various medical conditions. Without clinical studies, no medications would be available for use and they are only possible with the help of participants like you. Compensation varies by study and time involved, and whether you complete all visits and procedures in the study. Every volunteer study at CenExel CBH is approved and monitored by an Institutional Review Board (IRB) to make sure the risks are as low as possible and are worth any potential benefits to the volunteer.

Why does CenExel CBH need Healthy Volunteers?

Volunteers are an integral part of the research process. People with a particular disease as well as healthy people both can play a role in contributing to medical advances. Medical researchers can be provided valuable information when comparing healthy volunteers with those who have specific illnesses.

Medical research continues to bring new medication and treatments to help make all our lives better. The FDA requires clinical research, trials, or medical studies, to test the efficacy of these new drugs. CenExel CBH is a national leader in conducting these clinical research studies.

The main objective during a clinical trial on healthy volunteers is safety. Medical researchers need to determine how a certain drug is metabolized by the body. Drugs can be administered by a variety of routes depending on the intended site of action, drug metabolism, chemical properties of the medication and ease of use.

CenExel CBH needs healthy volunteers to participate in a variety of clinical trials, particularly for vaccines (e.g., RSV, HPV, etc.).

Clinical Trial Compensation

As medical research continues to bring new medication and treatments that help make all our lives better, healthy volunteers can experience the satisfaction of participating and assisting in the development these drugs. CenExel CBH compensates you for your time, travel, and participation in the study.

 
We have helped tens of thousands of patients in similar studies.
Space in this study is limited. To be considered, please fill out the form or call 301-251-4702.

STUDY DETAILS

Studies are currently available for qualified participants.

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No health insurance required

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Compensation for time and travel up to $1,000

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Male / Female

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18+ years old

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9318 Gaither Road, Ste 220
Gaithersburg, MD 20877

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State of the Art Facilities

CBH is Maryland’s premier clinical research organization. For a decade, we’ve helped improve the quality of life for everyone by researching new medications and treatments. Our state-of-the-art facilities are held to the highest standards of cleanliness and quality.

Board Certified Physicians

Your safety is our greatest concern. Every procedure at CBH is overseen by expert medical staff and performed by some of the most well-respected board-certified physicians in the industry, each with many years of experience in their respective specialties.

FDA Approved Procedures

Rest assured, you are not signing up for treatment with “experimental” methods. CBH only uses FDA approved methods as if you were at any other hospital or clinic. Our research is focused on the medication associated with those methods.

Frequently asked questions

View all FAQs

What is a CenExel Center of Excellence?

CenExel Centers of Excellence provide unparalleled medical and scientific support in the design and execution of clinical trials. Their attention to detail assures quality, reliable results and has helped CenExel to consistently achieve and exceed patient recruitment goals. They have conducted thousands of studies, the variety and complexity of which have resulted in a great depth of experience and insight for the principal investigators and research staff in each facility. CenExel Centers of Excellence deliver the engagement, expertise, and results to ensure that clients achieve their clinical research goals.

How do clinical trials work?

The study procedures and process will vary depending on the type of clinical trial you participate in. Before you begin a study, the process and all procedures for that study will be explained to you. Throughout the study, the Study Coordinator and the Principal Investigator will assist you and can answer any questions you have. They will check your health at the beginning of the trial, give you specific instructions for participating in the trial, monitor you carefully during the trial, and stay in touch with you after the study.

Some clinical trials involve more tests and doctor visits than you would normally have for your illness or condition. Your participation will be most successful if you carefully follow all instructions you are given and stay in contact with the research staff.

How safe are clinical studies?

There are many safeguards in place that all companies must follow when conducting clinical trials.

The Food and Drug Administration (FDA) is the regulatory agency that oversees all clinical research conducted in the United States. It is their responsible to protect the rights and as much as possible, the welfare of subjects participating in clinical trials. They ensure that data collected from clinical trials is of the highest quality and they are the agency that determines whether a new treatment should be sold in the US. Several organizations and individuals are governed by FDA regulations including clinical investigators, sponsors (the companies developing the treatments), Contract Research Organizations (companies that help conduct the studies), and Institutional Review Boards (groups that are responsible for ensuring the safety and welfare of study participants).

Good Clinical Practice (GCP) guidelines are another safeguard implemented to protect the safety of subjects. These guidelines encompass federal regulations and industry-accepted standards that govern clinical trials on humans. These regulations and standards apply to the conduct of the studies, record keeping, informed consent of subjects, collection of scientific data, and submission of information needed for the FDA to determine whether a new treatment should or should not be sold in the US. All companies must follow these guidelines when conducting clinical research.

An Institutional Review Board (IRB) is a committee that is formally tasked by an institution to review, approve, and monitor research involving human subjects. IRBs ensure that the risks to subjects are minimized; that subjects are adequately informed about the trial and the implications it will have on their treatment; that study protocols are modified, when necessary, to ensure safety; that risks are reasonable in relation to the anticipated benefits and the importance of the knowledge to be gained; that subject selection is equitable and that no classes of patients are discriminated against; that informed consent is obtained; that there is a provision for safety monitoring in the research plan; and that here are adequate provisions for the privacy and confidentiality for subjects and the data collected.

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