Atlantic Research Group
Atlantic Research Group (ARG) is a unique CRO with established roots and an agile approach, focusing on clinical trials in Oncology, Immunology, Neurology, and Medical & Biopharma Technologies. Since 2004, ARG has been committed to advancing care through operational excellence and innovation, with a strong track record of success including over 50 market authorizations and 85% repeat customer business. ARG emphasizes personalized, patient-first strategies, flexible services, and building long-term relationships with sponsors, investigators, and patients.
Industries
Nr. of Employees
medium (51-250)
Atlantic Research Group
Charlottesville, Virginia, United States
Products
Data Management
Comprehensive clinical trial data management services offered by Atlantic Research Group including database builds, locks, custom listings, data coding, and reconciliation.
Data Management/EDC
Clinical data management services including electronic data capture (EDC) solutions.
TrialVista
An industry-leading Clinical Trial Management System (CTMS) designed and developed by clinical research professionals, featuring 100% modular and completely customizable architecture.
TrialVista CTMS
A clinical trial management system providing real-time data access and data-driven trial management.
Medical & Biopharma CRO Services
Full-service clinical research organization (CRO) services specializing in surgical and interventional clinical studies, medical device trials, and biopharma development.
Atlantic Research Group Clinical Research Services
Full-service clinical trial CRO and clinical research services specializing in neurology, oncology, and immunology with a focus on rare diseases and patient-centric approaches.
Data Management
Comprehensive clinical trial data management services offered by Atlantic Research Group including database builds, locks, custom listings, data coding, and reconciliation.
Data Management/EDC
Clinical data management services including electronic data capture (EDC) solutions.
TrialVista
An industry-leading Clinical Trial Management System (CTMS) designed and developed by clinical research professionals, featuring 100% modular and completely customizable architecture.
TrialVista CTMS
A clinical trial management system providing real-time data access and data-driven trial management.
Medical & Biopharma CRO Services
Full-service clinical research organization (CRO) services specializing in surgical and interventional clinical studies, medical device trials, and biopharma development.
Atlantic Research Group Clinical Research Services
Full-service clinical trial CRO and clinical research services specializing in neurology, oncology, and immunology with a focus on rare diseases and patient-centric approaches.
Services
Study governance, timeline and budget management, cross-functional coordination, and sponsor-facing program leadership.
On-site and remote monitoring, SDV support, investigator oversight, and coordination to maintain protocol compliance and data quality.
Clinical safety oversight, protocol advisory, multisource data review, and identification of safety signals.
EDC build, eCRF construction, data cleaning, integration of lab and vendor data, and database lock support.
Statistical planning, generation of SDTM/analysis datasets, statistical analysis, and regulatory statistics support.
Safety data management, adverse event review and reporting, and coordination of safety assessments across vendors and sites.
Study governance, timeline and budget management, cross-functional coordination, and sponsor-facing program leadership.
On-site and remote monitoring, SDV support, investigator oversight, and coordination to maintain protocol compliance and data quality.
Clinical safety oversight, protocol advisory, multisource data review, and identification of safety signals.
EDC build, eCRF construction, data cleaning, integration of lab and vendor data, and database lock support.
Statistical planning, generation of SDTM/analysis datasets, statistical analysis, and regulatory statistics support.
Safety data management, adverse event review and reporting, and coordination of safety assessments across vendors and sites.
Expertise Areas
- Oncology clinical trial management
- Immunology clinical trial management
- Neurology and neurodegenerative disease trials
- Early-phase development and First-in-Man studies
Key Technologies
- Electronic Data Capture (EDC)
- Clinical Trial Management Systems (CTMS)
- Cloud-based SaaS clinical platforms
- eCRF design and SDTM/analysis dataset generation
News & Updates
ARG explores the possibilities of generative AI within clinical research to improve processes and outcomes.
ARG sponsored and attended the ALS/MND symposium to stay at the forefront of neurodegenerative research.
Celebrating 20 years of making an impact in clinical research with a focus on stability, standards, and accessibility.
ARG will be a sponsor at the NEALS Annual meeting, emphasizing its commitment to neurodegenerative disease research.
ARG collaborated with Humacyte on their HAV program, supporting vascular trauma studies and regulatory submissions.
ARG contributed to the development and FDA approval of Bivigam, a biologic for immunodeficiency.
ARG explores the possibilities of generative AI within clinical research to improve processes and outcomes.
ARG sponsored and attended the ALS/MND symposium to stay at the forefront of neurodegenerative research.
Celebrating 20 years of making an impact in clinical research with a focus on stability, standards, and accessibility.
ARG will be a sponsor at the NEALS Annual meeting, emphasizing its commitment to neurodegenerative disease research.
ARG collaborated with Humacyte on their HAV program, supporting vascular trauma studies and regulatory submissions.
ARG contributed to the development and FDA approval of Bivigam, a biologic for immunodeficiency.