---
title: Clinical Trial Patient Consent Form Template | Paperform
description: Professional clinical trial consent form for research sites. Covers medical history, study protocol, adverse events, biological samples, and future contact. Secure, customizable, compliant.
url: "https://paperform.co/templates/clinical-trial-patient-consent-form"
type: static
generatedAt: "2026-03-28T00:43:20.943Z"
---

[← Back to free form templates](/templates/)    ![Clinical Trial Patient Consent Form](https://img.paperform.co/fetch/f_webp/https://d3gw2uv1ch7vdq.cloudfront.net/content/form_templates/assets/clinical-trial-patient-consent-form.png)
    [Preview](https://_preview.paperform.co/ai-template/clinical-trial-patient-consent-form) [Use this template for free](/create?ai-template=clinical-trial-patient-consent-form)    [Consent & Permission Forms](/templates/category/consent-permission/)[Healthcare & Medical Forms](/templates/category/healthcare/) [Healthcare](/templates/industry/healthcare/)[Research](/templates/industry/research/) [Physician](/templates/role/physician/)[Nurse](/templates/role/nurse/)[Healthcare Administrator](/templates/role/healthcare-admin/)[Researcher](/templates/role/researcher/)     About this free form template
Conducting clinical research requires clear, comprehensive patient consent that meets regulatory standards while remaining accessible to participants. This **Clinical Trial Patient Consent Form** template provides research sites with a professional, HIPAA-aware framework for obtaining informed consent from study participants.

### Why clinical trial consent forms matter

Clinical trials depend on voluntary participation built on trust and transparency. A well-structured consent form protects both participants and research institutions by documenting understanding of study procedures, data usage, biological sample handling, and future contact preferences. Digital consent forms streamline the enrollment process while maintaining secure, auditable records.

### Built for research coordinators and clinical sites

This template covers all essential consent areas for clinical research: medical history access and disclosure, study protocol agreement, adverse event reporting procedures, biological sample collection and storage, and permissions for future research contact. Conditional logic adapts the form based on participant responses, and built-in validation ensures complete, accurate information.

With **Paperform**, your clinical trial site can customize this template to match your specific study requirements, IRB protocols, and institutional branding. The form works seamlessly across desktop and mobile devices, making it accessible for participants completing consent remotely or on-site.

### Workflow automation with Stepper

Connect this consent form to [Stepper](https://stepper.io) to automate your enrollment workflow. Route completed consents to research coordinators, trigger enrollment confirmations, update participant databases, notify study teams, and maintain audit trails—all without manual data entry.

For studies requiring formal documentation and signatures, integrate [Papersign](https://papersign.com) to automatically generate consent agreements from form submissions and collect legally binding eSignatures, keeping everything connected in one workflow.

Paperform's SOC 2 Type II compliance and data security features give research sites the confidence to digitize clinical trial consent processes while meeting regulatory requirements. Trusted by healthcare organizations worldwide, Paperform transforms complex consent procedures into streamlined, participant-friendly experiences.
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