CenExel Marlton, NJ
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All Current Studies

Alzheimer’s Disease

Alzheimer’s Disease

by | Aug 5, 2025 |

CenExel Marlton is seeking volunteers living with Alzheimer's disease to participate in our clinical trial. Alzheimer's disease is the most common form of dementia. It is a progressive disease beginning with mild memory loss and possibly leading to loss of the ability...

Bipolar Disorder

Bipolar Disorder

by | Jan 1, 2025 |

CenExel HRI is seeking volunteers living with bipolar disorder to participate in our clinical trial. Bipolar disorder is a mental health disorder that causes dramatic shifts in a person's mood, energy and ability to think clearly. Individuals with bipolar experience...

Obesity

Obesity

by | Feb 24, 2024 |

CenExel HRI is seeking volunteers living with obesity to participate in our clinical trial. Obesity is a highly prevalent chronic disease characterized by excessive fat accumulation or distribution that presents a risk to health. Obesity can lead to type 2 diabetes,...

Schizophrenia

Schizophrenia

by | Jul 18, 2023 |

CenExel HRI is seeking volunteers living with schizophrenia to participate in our clinical trial. Schizophrenia is a mental health disorder in which people interpret reality abnormally. Schizophrenia may result in some combination of hallucinations, delusions, and...

Depression

Depression

by | Jul 18, 2023 |

CenExel HRI is seeking volunteers living with depression to participate in our clinical trial. Depression is a common and serious medical illness that negatively affects how you feel, the way you think and how act. Depression causes feelings of sadness and/or a loss...

Type 2 Diabetes

Type 2 Diabetes

by | Jul 18, 2023 |

CenExel HRI is seeking volunteers living with type 2 diabetes to participate in our clinical trial. Type 2 diabetes is a chronic (long-lasting) health condition that affects how your body turns food into energy. With type 2 diabetes, your body doesn't use insulin well...

Hypertension

Hypertension

by | Jul 17, 2023 |

CenExel HRI is seeking volunteers living with hypertension to participate in our clinical trial. Hypertension, also known as high blood pressure, is when the pressure in your blood vessels is too high. The heart has to work harder to pump blood. Untreated,...

Birth Control or Contraception

Birth Control or Contraception

by | Jun 9, 2023 |

CenExel HRI is seeking healthy female volunteers to participate in our contraception clinical trial. Contraception, also known as birth control, is the use of medicines, devices, or surgery to prevent pregnancy. Some methods of birth control include, but are not...

Healthy Volunteers

Healthy Volunteers

by | Feb 24, 2023 |

CenExel HRI is seeking healthy volunteers to participate in our clinical trial. Healthy volunteers are individuals in general good health.

Generalized Anxiety Disorder

Generalized Anxiety Disorder

by | Feb 14, 2023 |

CenExel HRI is seeking volunteers living with generalized anxiety disorder to participate in our clinical trial. Generalized anxiety disorder (GAD) is excessive, ongoing anxiety and worry that are difficult to control and interfere with day-to-day activities....

Diabetic Peripheral Neuropathy

Diabetic Peripheral Neuropathy

by | Feb 13, 2023 |

CenExel HRI is seeking volunteers living with diabetic peripheral neuropathy to participate in our clinical trial. Diabetic peripheral neuropathy is a type of nerve damage that can occur if you have diabetes. It affects the feet and legs first, followed by the hands...

Opioid Addiction

Opioid Addiction

by | Feb 11, 2023 |

CenExel HRI is seeking volunteers living with opioid addiction to participate in our clinical trial. Opioid addiction, also known as opioid use disorder, is characterized by a powerful, compulsive urge to use opioid drugs, even when they are no longer required...

Volunteer for a Clinical Trial

If you are interested in one of our studies, simply click on Apply Now button to learn more or if you would like to inquire about upcoming clinical trials, please call Patient Recruitment at 888-437-4104 for more information between 7am - 5pm Monday - Friday.

Speak Your Truth.
No Expectations.*

*Ask your Coordinator or Rater
State-of-the-Art Facilities

CenExel HRI is one of our premier clinical research facilities in New Jersey. For over a decade, we’ve helped improve the quality of life for everyone by researching new medications and treatments. Our state-of-the-art facility is held to the highest standards of cleanliness and quality.

Board-Certified Physicians

Your safety is our greatest concern. Every procedure at CenExel HRI 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. CenExel HRI 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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