Clinical Med Research, of greater Chicago strives to complete medical research projects in a timely, accurate manner. Our staff is certified, and our clinicians are highly trained. Clinical Med Research, delivers exceptional quality and exemplary service. Our mission is to introduce advanced medical solutions previously unavailable to most independent research teams. Our certified staff, clinicians and expert physicians not only provide clinical expertise but also decades of combined research experience and training at the finest academic institutions in the nation. Clinical Med Research provides a safe environment for vast numbers of patients while still maintaining the highest level of professional integrity. Our goal is to exceed our client’s expectations at every time
About us
Clinical Med Research,of Chicago
Illinois is Proud to offer clinical trials management strategies for all levels of research. Clinical Med Research, is committed to optimal professional conduct of clinical trials, with an emphasis on patient safety. We take pride in advancing medical science, and our certified training staff, clinicians, and expert physician possess years of combined experience in research at premium academic institutions. Our work with pharmaceutical companies, CROs and our cooperative efforts provide our patients with advanced treatment in a safe environment. We strive to exceed our client’s expectations, and we make every effort to complete our research in a precise, dynamic timely manner.
Clinical Med Research, offers a number of expert services performed by clinicians & staff who possess decades of combined research experience. Services include:
WHAT WE DO
Facilitating clinical trials sites to pharmaceutical companies and CROs who conduct FDA-approved clinical trials in disease prevention and management.
Clinical Med Research, contributes to the advancement of medical science by managing clinical trials in pharmaceutical, medical devices and therapies. All trials are conducted under the most stringent, ethical FDA-approved guidelines and follow strict Institutional Review Board’s recommendation to ensure patient safety and confidentiality.
OUR Mission
OUR Vision
Clinicians, certified staff and expert physicians at CMR, carry a company-wide vision to contribute to the advancement of medical research. We provide management of all types of clinical trials (pharmaceutical, devise, therapeutic) which collectively further innovative medical science solutions. Our devotion and commitment to shaping the future of medical science now, and into the future, is unwavering. We take pride in our accurate and timely completion of clinical trials and hold ourselves to the highest level of professional medical integrity. Our major priority is, and always will be, the safety of our patients, and we will constantly strive to maintain a safe, professional, environment for all who trust us with their health and lives.
OUR FAQs
Clinical Research Associate like ours is usually registered in pharmaceutical or CROs database to receive new trials on a regular basis. Therefore, are always interested in people who want to volunteer for future trials. If you or anyone you know is interested; don’t hesitate to contact our office at 561-573-8521 or email us at: info@clinicalmedresearch.com.
Medical scientists work tirelessly on a daily basis to uncover new information about medical conditions and possible therapeutics; in the form of drugs, medical devices, or techniques that can enhance the treatment outcome for a particular illness. With help of their new discovery you and many other people may benefit simply by the fact that you are willing to be involved.
There are lots of benefits in participating in a trial:
• Being involved in clinical studies could help in the development process of new medications, devices or equipments.
• You will be among those to receive investigational therapies before they are available to the general public.
• You are participating in an active role in your health care.
• Your participation will entitle you to receive free study medications and comprehensive monitoring at no cost to you by participating in a clinical trial.
• You may be entitled to receive financial compensation for your time and travel
As a volunteer or subject, you are entitled you exactly the nature of the study that you are about to enrolled in. Therefore, every volunteer will be presented with an Informed Consent that is designed to give volunteers the information that they need to make a decision about participating in a clinical research study. This essential process allows the volunteer to ask questions, express concerns and to exchange information freely with the clinical investigator. The clinical investigator also known as Principle Investigator is responsible to make sure that informed consent is obtained from each research volunteer according to the proper protocol before that person participates in the research study.
It is against FDA ethical rules to bribe or convince any volunteer to participate in a clinical trial against their will. Volunteering is a personal choice that you can make to join a study. You are always entitled to say no, should you feel uncomfortable about the practice, the medication you are receiving or the study in general.