Current Clinical Trials
Adult ADHD, Ages 18-55
To learn more, please contact
Dana Hauser or Emily Lindenbaum
or by phone at (248) 608 8800 ext. 226 or 248
Please click here to fill out our research contact form.
Study topics change frequently, so check back often!
RCBM conducts FDA mandated research studies for the evaluation of investigational medications. These studies are undertaken to assess the safety and effectiveness of these medications. If in the aggregate the medications are deemed acceptable by the FDA, they are ultimately released to the general public. Our research team works in collaboration with pharmaceutical companies to study medication-based treatments for various conditions. All of these studies are highly regulated by independent third parties. Still have questions? Please visit https://clinicaltrials.gov/
Glossary of Commonly Used Terms
Click here for the Glossary PDF
About the Clinical Trials Group
The Clinical Trials Group at RCBM conducts FDA mandated research studies for the evaluation of investigational medications or new indications for existing medications. These studies are undertaken to assess the safety and effectiveness of these medications. If in the aggregate the medications are deemed acceptable by the FDA, they are released to market for consumers. Our Clinical Research team works in collaboration with pharmaceutical companies to study medication-based treatments for various conditions. All of these studies are highly regulated and monitored continuously by independent third parties.
Meet Our Professionals
Joel L. Young, MD, Principal Investigator the Clinical Trials Group, Medical Director of RCBM
Lori Niewiarowski BS, GCRAD, Clinical Research Project Manager
Lori Niewiarowski is the Research Project Manager, Rater and Clinical Research Coordinator at the Clinical Trials Group. She graduated from Madonna University with a Bachelor of Science in Psychology. She comes to RCBM with over 10 years experience in patient care, which includes Henry Ford health systems and the Detroit Medical Center. She also graduated from Eastern Michigan University with a Master’s in Clinical Research. Lori has extensive experience with conducting clinical research in various specialties. Her main focus is ethics and clinical trial management with emphasis in quality control.
Dana Hauser, BS, Clinical Research Coordinator & Regulatory Specialist
Dana Hauser is a senior research staff member at the Clinical Trials Group. Dana has over 11 years experience in healthcare including clinical research, healthcare administration, and patient care, spanning multiple health systems in Michigan and out of state. She graduated from Kaplan University with a Bachelor of Health Science and Nutrition. Dana is currently working on her thesis to complete her Masters of Administration and Management from Central Michigan University. At CTG, Dana enjoys coordinating and managing research trials for adults and adolescents in a variety of CNS and sub-specialty areas of study. In addition, Dana has generous knowledge of the geriatric population, specifically in nephrology and cardiac related clinical research studies.
Emily Lindenbaum BBA, Clinical Research Coordinator, Marketing & Recruitment Specialist
Emily is an administrative marketing and advertising professional in healthcare and business who supports the ethical and confidential considerations related to research and good clinical practice. Emily coordinates technical assistance, clinic visits and recruitment responsibilities for Clinical Trials at RCBM. She is training to become a rater for CNS trials. She has a Bachelors of Business Administration in Marketing at Grand Valley State University. She is currently working to apply for her Masters in Art Therapy & Education to conduct group therapy sessions.