Highly rated by customers | 4.2 / 5 stars
Patient Recruitment software for clinical research
ResearchManager Patient Recruitment supports efficient and compliant recruitment of clinical research participants. Patients easily register themselves via a QR code or link, while research teams maintain real-time visibility into progress and response rates.
- Up to 35% higher response rate through self-registration via QR code or link
- Up to 40% higher response rate through social and digital campaigns
- Up to 50% higher response rate with mobile-friendly registration
Fully compliant with relevant laws and regulations
Self-registration via QR code or website
With ResearchManager Patient Recruitment, patients can register directly via a QR code or Web page. Placing QR codes on patient information or consent forms lowers the barrier to participation.
Sharing through social media and digital campaigns
Study invitations can be easily distributed through social media and other digital channels to reach a wide and targeted audience. Through a shared link, potential participants get direct access to the registration page.
Verification and acceptance of applications
All incoming applications can be reviewed by the research team before participants are admitted to the study. In addition, it is possible to automatically accept applications based on preset selection criteria.
Key Features
Digital recruitment and inclusion
- Direct self-registration via QR code or unique study link
- Mobile-optimized registration forms
- Dissemination through social media and targeted digital campaigns
- Configurable landing pages per study
- Support for multicenter recruitment
- Real-time insight into response rates and conversion
Controlled selection and screening
- Manual or automated participant acceptance
- Selection based on predefined inclusion criteria
- Overview of enrollment status and screening by participant
- Configurable workflows for screening and follow-up
- Automated notifications and communication
Compliance, security & integrations
- Role-based access rights
- Support for Single Sign-On (SSO)
- Two-factor authentication
- Validated electronic signatures
- Full audit trail of all actions
- Compliant with FDA 21 CFR Part 11 and ICH-GCP
- Secure data storage in compliance with ISO 27001, GDPR, HIPAA, and NHS Data Security & Protection Toolkit
- Import and export capabilities in various formats
- REST API for reading and writing data
Trusted by 200+ organizations
For more than 13 years, CROs, sponsors, universities and healthcare organizations have relied on Clinical Research Suite every day for structured and reliable clinical research. Find out how we help organizations conduct studies more efficiently, compliantly and with complete control.