Women’s Health Studies
Our expertise lies in evaluating the safety and efficacy of investigational new drugs, products, and procedures for the treatment of gynecological disorders affecting the health and quality of life of women throughout various stages of life.
CITrials has a great reputation for producing clinical trial results accurately, quickly and with adherence to global guideline requirements. CITrials has a team of board-certified physician/researchers affiliated with Southern California’s leading universities and hospitals. These investigators partner with other skilled CITrials staff to perform both inpatient and outpatient studies working with central IRBs to eliminate the need for subsequent medical reviews.
CITrials has a dedicated team to recruit and retain patients from diverse ethnic populations across Los Angeles, Orange, and Riverside/San Bernardino counties. CITrials employs a highly collaborative process between staff and community hospitals, mental health organizations and doctors to identify participants for clinical trials. The clinical trials are confidential, volunteers DO NOT insurance, and are provided compensation for their time and travel.
Volunteer for a Clinical Trial
If you are interested in one of our studies or would like to inquire about upcoming clinical trials, please call Patient Recruitment for more information between 8:30AM - 4:30PM Monday - Friday.
Call 732-341-9500 now or fill in the form below and we will contact you:
Qualified participants will receive free medical care related to the study and may receive financial compensation for time and travel expenses. Enrollment is limited.
Please call 732-341-9500 for details or fill out the form above.
AMRI is New Jersey's premier clinical research organization. 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.
Your safety is our greatest concern. Every procedure at AMRI 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.
Rest assured, you are not signing up for treatment with “experimental” methods. AMRI 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
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.