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Explore all the solutions you can create with Paperform: surveys, quizzes, tests, payment forms, scheduling forms, and a whole lot more.
See all solutions
Connect with over 2,000 popular apps and software to improve productivity and automate workflows
See all integrations
Finding the right clinical trial can be challenging. Our Clinical Research Study Recruitment Newsletter connects you with relevant research opportunities tailored to your specific health conditions and preferences.
This newsletter form goes beyond basic email sign-ups. By sharing your condition interests, trial phase preferences, and basic eligibility information, you'll receive:
Whether you're a clinical research organization (CRO), hospital research department, pharmaceutical company, or academic medical center, Paperform makes it easy to build targeted recruitment lists and streamline participant outreach.
Smart conditional logic ensures subscribers only see questions relevant to their situation, while secure data collection keeps sensitive health information protected. Connect this form to your CRM or email marketing platform through Stepper to automatically segment subscribers by condition, create targeted campaigns, and trigger personalized follow-up workflows.
For organizations managing multiple studies, you can duplicate this template for different therapeutic areas, embed it across multiple recruitment sites, and maintain SOC 2 Type II compliant data collection that research teams can trust.
Stop relying on scattered spreadsheets and manual list management. This form template integrates seamlessly with your existing tools—sync subscribers to HubSpot, Mailchimp, or your research database, and use Stepper workflows to automatically notify study coordinators when qualified candidates sign up.
With over 500,000 teams trusting Paperform for secure, GDPR-compliant data collection, you can focus on advancing medical research while we handle the technical details of subscriber management and data integration.
A comprehensive advocacy form for individuals and caregivers to share their experiences, express interest in clinical trials, and raise concerns about memory care facility quality while supporting Alzheimer's research initiatives.
Newsletter subscription form for families with loved ones in assisted living, featuring care updates, billing preferences, and visit scheduling options.
A comprehensive research study enrollment form for families with children eligible for autism early intervention programs, including developmental milestone tracking, therapy commitment assessment, and parental consent.
A comprehensive registration form for participants joining a bipolar disorder medication adherence research study, including consent for mood tracking, pharmacogenetic testing, digital monitoring, and hospitalization prevention planning.
A comprehensive enrollment form for celiac disease research studies involving gluten challenge protocols, with consent sections for antibody testing, endoscopy procedures, symptom monitoring, and strict follow-up requirements.
Request access to patient genomic test data, variant interpretations, family history, and genetic counseling notes from clinical genomics laboratories.
Gather feedback from clinical trial participants about their experience with study coordination, consent processes, communication, and overall satisfaction to improve research operations.
Screen and verify potential clinical study participants with age verification, comprehensive health screening questions, and informed consent documentation.
Complete clinical trial enrollment form with eligibility screening, informed consent, appointment scheduling, and compensation details. Streamline your research participant enrollment process.
Verify participant age and eligibility for clinical trials with integrated consent forms and HIPAA authorization for compliant healthcare research enrollment.
A comprehensive emergency contact form for clinical trial participants, including study coordinator information, adverse reaction protocols, and 24/7 emergency support details.
Verify participant identity, eligibility, and collect essential medical information for clinical trial enrollment with integrated consent and screening.