Jed Kaminetsky, M.D. / Principal Investigator
Betsy Ortiz Moclair,, RN CCRC / Clinical Trials Manager
University Urology Associates
215 Lexington Avenue, 20th Floor
New York, NY 10016
212-686-9015 or 212-686-9015 ext 9
University Urology Associates is a private urology practice with a dedicated research site proficient in Phase II-IV clinical trials, under the supervision of Dr. Jed Kaminetsky, a Board Certified Urologist. University Urology is located in New York City, a large metropolitan area. Our location allows for us to partner with many other private practice physicians to augment recruitment of subjects. Additionally, we have a robust outreach program to further assist with recruitment of subjects. Our extensive industry experience enables us to offer our sponsors a quality research site with a trained and experienced clinical research team.
Experience in + 100 Clinical Research Trials involving the following therapeutic areas:
University Urology is an outpatient facility located in Midtown Manhattan. Our equipment and capabilities include:
Dr. Jed Kaminetsky, M.D. is a Clinical Associate Professor at New York University Medical Center, Associate medical Director of Gramercy Surgical Centre and is a practicing urologist with University Urology Associates, one of the largest urologic practices in the New York City metropolitan area. He is a board certified urologist and is highly skilled in treating all urologic disorders, performing minimally invasive prostate surgeries and penile implants. Dr. Kaminetsky's academic interests include the study of both male and female sexual dysfunction, which has led him to become a national and world thought leader. Dr. Kaminetsky work has been published in several journals which led to a nationwide recognition and development of various treatment schemes for patients with sexual, erectile dysfunction and androgen deficiency. Moreover, Dr. Kaminetsky is an experienced principal investigator who participates in national research studies that explore pharmacologic and diagnostic techniques for various urologic disorders. He is currently conducting studies addressing premature ejaculation, ED, male and female sexual dysfunction, BPH, prostate cancer, bladder cancer, voiding dysfunction, and hypogonadism. His hospital appointments include New York University Medical Center, New York Downtown Medical Center. Dr. Kaminetsky has been consulting for several pharmaceutical companies including Slate, Pfizer, Auxilium, Lilly, GlaxoSmithKline and American Medical Systems.
Betsy Ortiz Moclair, RN, CCRC, BSN is the Clinical Trials Director and registered nurse for University Urology Associates. Betsy has over 15 years of experience in clinical research. Her responsibilities include directing and conducting all managerial and operational aspects of all clinical trials. In addition to clinical research, she obtains a thorough medical history for incoming new patients. Betsy works in close contact with all the principal investigators, including Dr. Kaminetsky, to ensure that all patients are receiving the best quality of care. She has been actively involved in over 100 clinical trials.
University Urology Associates has a full-time ACRP Certified Clinical Trials Manager/CCRC, a Certified Clinical Research Coordinator, a study enrollment recruiter, and two research assistants. The staff is experienced in working with Sponsors, CROs, and the Central IRB to ensure integrity of study, patient safety, accurate data collection, and timely document submission.
Our study team is fully trained and up to date in the handling and shipping of biological/biohazard substances in accordance with U.S. Department of Transportation (DOT) and International Air Transportation Association (IATA) Dangerous Goods Regulations.
Furthermore, each member of our study staff has received formal training in:
We are also proficient in a wide variety of electronic data capture systems, which include:
Our location in Manhattan exposes us to a wide variety of patient demographics. New York City is the largest city in the United States with a population of more than 8 million people. This allows for compliance with FDA standards for ethnically and racially diverse subject expectations. We are centrally located and in close proximity to public transportation allowing for easy access for our subjects and sponsors visits.
University Urology Associates utilizes a Central IRB. Regulatory documents are completed within 5 days, allowing for a quick turnaround. All case report data is entered shortly after subject visit has been completed. In addition, we frequently check all data systems on a daily basis, allowing for a fast turnaround of query resolution.