At 3SYNC Research, we are committed to fostering connections between our valued partners and the communities we serve. Whether you’re an Investigator, Sponsor, CRO, or Participant, our mission is to support your journey through the clinical research process, ensuring success and making a difference together.
Bringing research opportunities to diverse and underserved communities
3SYNC Research is a rapidly growing network of fully integrated clinical research sites in the United States. We increase access to clinical trials in underserved communities, support new investigators entering the industry, and partner with pharmaceutical and biotechnology companies as well as contract research networks.
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.
Our dedicated staff of seasoned professionals and our partners
3SYNC studies are led by seasoned investigators and experienced site staff. Our investigators and multilingual clinical teams are committed to working together with sponsors, CROs, and partners through all phases of clinical research. Our Investigators include primary care doctors, specialists, and nurse practitioners with extensive clinical experience.
Our strategic advantages include our data quality and related recruitment capacity. We provide quality data using customized tools that include our CTMS, data capabilities, and SIFTA™ subject screening software. We also use advanced software solutions for eRegulatory, eSource, and remote data management.
3SYNC Research provides the highest level of site research, quality study data and new investigator mentoring
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.
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.
Our strategic edge lies in delivering high-quality data and robust recruitment through customized tools like CTMS, SIFTA™, and advanced eRegulatory and eSource solutions.
Our recruitment expertise, backed by nearly 3 million patient records and a 91% retention rate, is driven by our GCP-certified specialists' patient-centric approach and thorough interactions.
Our centralized site network streamlines feasibility, business development, and regulatory processes, enabling us to negotiate a single budget and contract for all sites.
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.
At 3SYNC Research, we are continuously expanding our network by adding new clinical trials and partnering with more investigators, physicians, and healthcare professionals. We are always looking to collaborate with dedicated medical experts who share our commitment to advancing research and improving patient outcomes.
Shared successful experiences
At 3SYNC Research, our strength lies in our seasoned investigators, experienced bilingual staff, and advanced data management tools. Our diverse team of primary care doctors, specialists, and nurse practitioners bring extensive clinical expertise, allowing us to conduct comprehensive trials across various therapeutic areas. We excel in data quality, using customized solutions like CTMS, and SIFTA™ to ensure accurate and reliable results. Our recruitment capabilities are unmatched, supported by a database of nearly 4 million patient records and a 95% retention rate, thanks to our GCP-certified, patient-centric recruitment specialists. With a centralized site network model, we streamline feasibility, contracts, and regulatory processes, offering expedited study start-up timelines and efficient trial management. This combination of expertise, quality, and efficiency defines "The 3SYNC Advantage."