Science 37

Overview

Science 37 is a clinical research company based in the United States, founded in 2014. It specializes in decentralized clinical trials (DCTs) by utilizing telemedicine and proprietary technology platforms like Metasite™ and NORA. The company aims to enhance trial enrollment, improve patient access and diversity, and ensure data quality while reducing costs and geographic barriers. Science 37 operates as the first FDA-inspected Direct-to-Patient Clinical Trial Site and has facilities in Research Triangle Park, North Carolina, and previously in Culver City, California.

The organization provides end-to-end solutions through a unified technology stack, employing board-certified investigators and research-grade nurses. Its Metasite™ platform allows patients to participate in trials from home, utilizing features such as eConsent and telemedicine. Science 37 also offers a tech-driven patient recruitment solution to streamline the enrollment process and has partnered with major pharmaceutical firms, including Novartis and Amgen, to support various clinical trials across multiple therapeutic areas.

Basic Information

Contact Details

• Phone: +1 984-377-3737
• Website: science37.com
• LinkedIn: linkedin.com/company/science-37

Key Focus Areas & Initiatives

• Site conduct
• Clinical trial access
• Clinical trial enrollment
• Patient qualification
• Patient recruitment
• Direct-to-patient clinical trials
• Hybrid clinical trials
• Remote clinical trials
• Decentralized clinical trials
• Real-world evidence
• Clinical trial data integrity
• Clinical trial support
• AI recruitment
• Remote diagnostics
• Clinical trial compliance
• Remote neurology
• Digital health regulatory
• Clinical data capture
• Remote patient engagement
• Site-less trials
• Remote cardiology
• Clinical research innovation
• Telehealth
• Regulatory guidance
• Clinical trial automation
• AI-driven feasibility assessment
• Contract research organizations (CROs)
• Digital health tools
• Metasite rescue
• Remote infectious disease
• Patient journey automation
• Patient-centric approach
• AI algorithms
• Data integration
• Digital health innovation
• Patient outreach
• Clinical trial management
• Data collection
• Remote dermatology
• Patient onboarding
• Patient diversity
• Remote data collection
• Pharmaceuticals
• Digital biomarkers
• Virtual trial site
• Clinical trial efficiency
• Global patient access
• Remote trial management
• Regulatory compliance
• AI-powered insights
• Remote patient consent
• Virtual site
• Virtual trial monitoring
• Network oriented research assistant (NORA)
• Global access
• Remote monitoring
• Trial acceleration
• Clinical trial technology
• Social determinants of health
• Remote endpoint data collection
• Clinical trial analytics
• Clinical trial reporting
• Telemedicine
• Patient experience optimization
• Patient retention
• Cloud platform
• Clinical data management
• Digital health ecosystem
• Metasite™ virtual site
• Digital health integration
• Remote trial conduct
• Remote patient care
• Data security
• Metasite
• Trial speed
• Virtual trial compliance
• Healthcare technology
• Digital health engagement
• Trial efficiency
• Patient portal
• Study management
• Remote patient safety
• Biotechnology
• Patient diversity enhancement
• Econsent
• Decentralized trials
• Connected devices
• Digital health training
• Regulatory strategy
• Remote trial recruitment
• High-quality data
• Clinical trial software
• Clinical trial services
• Digital data collection
• Social determinants of health in research
• Remote oncology
• Diversity in trials
• Digital consent
• Site-less research
• Medical and diagnostic laboratories
• Patient-centric trials
• Patient engagement
• Digital biomarkers in trials
• Digital health solutions
• Real-world evidence
• Virtual clinical trial infrastructure
• Hybrid trial models
• Digital health records
• Digital health literacy
• Remote rare disease
• Virtual trial platform
• Therapeutic areas
• B2B
• AI-driven recruitment
• Clinical trial platform
• Remote patient monitoring
• Social determinants data
• Remote site management
• Digital health
• Patient experience
• Mobile app
• Virtual clinical trials
• Hybrid research
• Clinical research
• Protocol compliance
• CRO support
• Mobile healthcare
• Investigator recruitment
• Flexible treatment options
• Clinical trial acceleration
• Diversity in clinical trials
• Centralized patient engagement
• Electronic data capture
• Study orchestration
• Clinical trial participation
• Patient-centric research
• Omnichannel recruitment
• In-home patient visits
• Community provider partnerships
• Medical records retrieval
• GCP standards
• Endpoint data collection
• Patient-first experience
• Research site integration
• Centralized enrollment
• Data-driven feasibility
• Participation barriers
• Inclusive research models
• Therapeutic area expertise
• Trial activity spectrum
• Trained healthcare staff
• Historical enrollment patterns
• Patient experience improvement
• Participatory research methods
• B2C
• Education
• Information technology & services
• Health, wellness & fitness
• Hospital & health care
• Enterprise software
• Enterprises
• Computer software
• Medical
• Computer & network security
• Medical & diagnostic laboratories
• Medical practice

Technologies Used

• Amazon SES
• Atlassian Cloud
• Drift
• Five9
• Gmail
• Google Apps
• LEAP
• MailChimp SPF
• Marketo
• Microsoft Office
• Microsoft Office 365
• Mimecast
• NetSuite
• OnCore CTMS
• OneTrust
• React
• React Redux
• Remote
• Route 53
• Salesforce
• Slack
• Veeva Vault eTMF

Affiliated Organizations & Regional Branches

• eMed