3SYNC is Led by top-tier Investigators and Physicians
Our expertise defines our distinction.
Expanding Access to Advanced Clinical Research
About Us
What Makes 3SYNC Unique
3SYNC Research is a rapidly growing organization of fully integrated clinical research sites in the United States. We increase access to clinical trials in underserved communities, and support new investigators entering the industry, while partnering with pharmaceutical and biotechnology companies, and contract research organizations.
3SYNC Research strives to bring clinical trial opportunities to diverse communities. Through growth, acquisitions, and partnerships with doctors, 3SYNC offers patients with unmet needs access to care and clinical research.
We aim to serve our research subjects, grow our partnerships, and support the execution of trials that adhere to all regulations governing research including the FDA Code of Federation Regulations (CFR), with particular attention to the most recent FDA diversity mandates in research conduct.
Our Capabilities
3SYNC Research provides the highest level of site research, quality study data and new investigator mentoring
01
Our Investigators
At 3SYNC Research, our experienced, multilingual teams collaborate with sponsors and diverse healthcare professionals to conduct comprehensive clinical trials that advance research and serve diverse communities.
02
Staff Experience
With over 30 experienced, bilingual staff and diverse principal investigators, 3SYNC conducts trials across various indications and therapeutic areas, supported by decades of research expertise.
03
Data Quality
Our strategic edge lies in delivering high-quality data and robust recruitment through customized tools like CTMS, SIFTA™, and advanced eRegulatory and eSource solutions.
04
Subject Recruiting
Our recruitment expertise, backed by nearly 4 million patient records and a 95% retention rate, is driven by our GCP-certified specialists' patient-centric approach and thorough interactions.
05
Central Coordination
Our centralized site network streamlines feasibility, business development, and regulatory processes, enabling us to negotiate a single budget and contract for all sites.
06
Responsiveness
Responsiveness is at the core of our operations. We prioritize swift and effective communication, ensuring that our partners, investigators, and participants receive support and solutions at every stage of the process.
Dedicated Experts Committed to Advancing Clinical Research
Meet Our Team
Our Experience Speaks Volumes
Jerome R. Obed, MD
Principal Investigator
With a distinguished background in Dermatology, Neurology, Internal Medicine, and Infectious Diseases, boasting over 25 years of clinical research experience and numerous publications and leadership roles, he has made significant contributions to advancing medical research.
Marcus Sevier, PA-C, MHA
Sub-Investigator
Director research activities in Texas, serves as a Sub-Investigator, and brings over 20 years of experience in Family Medicine, Urgent Care, Occupational Medicine, and clinical research across multiple therapeutic areas.
Danielle Neuman, MD
Diabetes & Metabolism Endocrinologist
Dr. Danielle Neuman is a board-certified internist and specialist in Endocrinology. Dr. Danielle Neuman has evaluated and treated numerous patient Populations throughout her experience allowing her the opportunity to exercise her intellectual curiosity in medicine.
Join Our Research Network
Investigators and Physicians, complete the form to collaborate and advance medical innovation!
