
Patient RecruitmentScience 37
Science 37 Patient Recruitment accelerates clinical trial enrollment by delivering medically qualified, site-ready participants through predictive modeling, clinician oversight, and real-world data. It improves referral quality, reduces site burden, and enhances retention with patient-centric engagement strategies.
Vendor
Science 37
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Product details
Patient Recruitment
Science 37 Patient Recruitment is a results-driven solution designed to accelerate clinical trial enrollment by delivering medically qualified, site-ready participants. Leveraging real-world data, predictive modeling, and clinician oversight, it ensures high-quality referrals that reduce site burden, improve retention, and keep trials on schedule.
Features
- Medical Record-Qualified Referrals: Every patient is pre-screened using medical records to confirm eligibility.
- Clinician-Reviewed Screening: Internal investigators and research-grade nurses validate participant readiness.
- Dual Enrollment Pathways: Patients can choose to participate at a traditional site or remotely from home.
- Omni-Channel Outreach: Combines digital, physical, and provider-based engagement to reach diverse populations.
- Heatmapping Technology: Identifies patient clusters and their treating physicians for targeted recruitment.
- Patient Engagement Coordinators: Support participants throughout their journey to improve retention.
- Rapid Turnaround: Average 3-day medical record processing to accelerate enrollment timelines.
- Site Engagement Support: Designed to integrate seamlessly with brick-and-mortar research sites.
Capabilities
- End-to-End Recruitment Workflow: From identification and prequalification to consent and clinical review.
- Predictive Modeling: Uses a proprietary database of over 6 million patients to identify ideal candidates.
- Integrated Outreach Strategy: Combines patient advocacy, provider engagement, and precision targeting.
- Results-Based Pricing: A performance-driven model that minimizes sponsor risk.
- Scalable Deployment: Supports trials of varying sizes and therapeutic areas.
- Patient-Centric Design: Focuses on accessibility, choice, and comfort to enhance participation.
Benefits
- Accelerated Enrollment: Reduces delays by delivering study-ready participants.
- Improved Referral Quality: Eliminates unqualified leads, saving time and resources.
- Higher Retention Rates: Personalized support and flexible participation options improve patient engagement.
- Reduced Site Burden: Sites receive only pre-qualified referrals, streamlining operations.
- Enhanced ROI: Efficient recruitment processes lead to faster trial completion and cost savings.
- Expanded Access: Reaches underrepresented and remote populations, improving trial diversity.