Clinical Trial Informed Consent Form Google Form Template

Consent & Waiver6 minUpdated

A free Google Form template for clinical trial participant consent. Streamline study enrollment, document risks and benefits, and capture signatures.

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Embedded Google Form. Scroll inside the frame to see all questions.

About this template

A Clinical Trial Informed Consent Form is an essential document for clinical researchers, medical professionals, and study coordinators gathering voluntary agreement from participants before beginning a study, drug trial, or medical device evaluation. This template ensures that potential participants fully understand the study's purpose, potential risks and benefits, confidentiality measures, and their absolute right to withdraw at any time without penalty.

Designing this document as a digital form allows participants to review terms and submit their acknowledgments seamlessly across mobile phones, tablets, or computers. Researchers can quickly track study enrollments, organize participant acknowledgments, and maintain clear audit trails for regulatory compliance. With Doc2Form, you can instantly turn this structured layout into a working Google Form to streamline your onboarding workflow.

Key features

  • Capture participant consent and acknowledgments digitally in one secure place.
  • Clearly outline trial risks, benefits, and participant withdrawal rights.
  • Include dedicated signature and date fields for participants, agents, and witnesses.
  • Easily accessible on any device for remote or in-person study enrollment.
  • Instantly deployable as a Google Form using Doc2Form.

Use cases

  • Pharmaceutical drug trials and medical device evaluations.
  • Academic and clinical research studies involving human subjects.
  • Specialized therapeutic procedures requiring documented patient consent.

What this form collects

  • Participant Full Name (Short answer)Enter your first and last name as it appears on official identification.
  • Participant Date of Birth (Date)Provide your date of birth for participant verification.
  • Confirmation of Study Briefing (Multiple choice)Confirm that a researcher has explained the clinical trial purpose, procedures, potential risks, and expected benefits to you.
  • Acknowledgment of Voluntary Participation (Multiple choice)Acknowledge that your participation is entirely voluntary and that you may withdraw at any time.
  • Participant Signature (Paragraph)Please paste a link to your signed consent document or type your full legal name as an electronic signature.
  • Participant Date Signed (Date)Select today's date.
  • Did an agent assist with this consent process? (Multiple choice)Select whether a legal representative or authorized agent assisted the participant.
  • Agent Name (Short answer)Enter the full name of the assisting agent or legal representative, if applicable.
  • Agent Signature (Paragraph)Agent electronic signature or document link.
  • Agent Date Signed (Date)Date of agent sign-off.
  • Witness Name (Short answer)Enter the full name of the impartial witness observing the consent process, if required.
  • Witness Signature (Paragraph)Witness electronic signature or document link.
  • Witness Date Signed (Date)Date of witness sign-off.
  • Lead Researcher Name (Short answer)Enter the name of the principal investigator or researcher obtaining consent.
  • Lead Researcher Signature (Paragraph)Researcher electronic signature or document link.
  • Lead Researcher Date Signed (Date)Date of researcher sign-off.

FAQ

What is a clinical trial informed consent form?

It is a vital document that outlines the details of a medical study, ensuring participants fully understand the procedures, risks, benefits, and their rights before agreeing to take part.

Why is proper informed consent documentation important?

It protects both the participant and the research institution by verifying that consent was given voluntarily, ethically, and with full comprehension of the study requirements.

Can participants withdraw their consent after signing?

Yes, participants retain the right to withdraw from a clinical trial at any time without penalty or loss of benefits to which they are otherwise entitled.

How can I deploy this form for my study participants?

With Doc2Form, you can instantly convert this template into a fully functional Google Form to collect digital responses and manage your research pipeline efficiently.

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Save a copy to your Google Drive with one click (uses 1 credit). Or build from a PDF or description in the app.

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