3Sync
3SYNC Research is a rapidly growing network of fully integrated clinical research sites in the United States, committed to increasing access to clinical trials in underserved communities, supporting new investigators, and partnering with pharmaceutical, biotechnology companies, and contract research organizations. They focus on bringing clinical trial opportunities to diverse communities, supporting research subjects, and ensuring trials adhere to all regulations, including FDA mandates. Their mission emphasizes innovation, access, and compassion in healthcare.
Industries
Nr. of Employees
medium (51-250)
3Sync
Services
Full-service site operations including participant visits, safety oversight, protocol implementation, and site staffing for clinical studies.
Training programs and mentorship to onboard sub-investigators and support progression to principal investigator roles, including regulatory and ethical training.
Targeted recruitment using an internal patient database and multilingual outreach, plus retention management including participant communications and follow-up.
Centralized feasibility, budgeting, and contracting across network sites to accelerate study start-up and simplify sponsor interactions.
Regulatory document management, protocol support, and compliance oversight aligned with federal regulations and GCP to support IRB and agency requirements.
Implementation and management of CTMS, eRegulatory, and eSource systems to capture, store, and monitor study data in near real-time.
Full-service site operations including participant visits, safety oversight, protocol implementation, and site staffing for clinical studies.
Training programs and mentorship to onboard sub-investigators and support progression to principal investigator roles, including regulatory and ethical training.
Targeted recruitment using an internal patient database and multilingual outreach, plus retention management including participant communications and follow-up.
Centralized feasibility, budgeting, and contracting across network sites to accelerate study start-up and simplify sponsor interactions.
Regulatory document management, protocol support, and compliance oversight aligned with federal regulations and GCP to support IRB and agency requirements.
Implementation and management of CTMS, eRegulatory, and eSource systems to capture, store, and monitor study data in near real-time.
Expertise Areas
- Clinical trial management
- Patient recruitment and retention
- Investigator training and site development
- Regulatory compliance and GCP
Key Technologies
- Clinical trial management systems (CTMS)
- Electronic regulatory systems (eRegulatory)
- Electronic source data capture (eSource)
- Subject screening and pre‑screening software
News & Updates
An overview of the safety measures, regulatory oversight, and participant protections in place for clinical trials in 2025, emphasizing transparency, ethics, and advanced monitoring technologies.
Information on how Florida residents can participate in clinical trials, earn compensation up to $5,000, and access free care and treatment without insurance.
Latest news, research updates, and insights from 3SYNC Research, including guides on trial safety and participation benefits.
An overview of the safety measures, regulatory oversight, and participant protections in place for clinical trials in 2025, emphasizing transparency, ethics, and advanced monitoring technologies.
Information on how Florida residents can participate in clinical trials, earn compensation up to $5,000, and access free care and treatment without insurance.
Latest news, research updates, and insights from 3SYNC Research, including guides on trial safety and participation benefits.