Parties & Scope
Identify each party by legal name and describe the study scope, locations, and activities covered by the agreement.
A formal Educational Study Contract protects participant privacy, allocates legal responsibility, documents data access and retention, and clarifies funding and publication rights. It reduces regulatory risk, supports IRB review, and creates an enforceable record of consent and obligations for all parties.
Multiple campus and project roles use this contract to align legal, ethical, and operational requirements.
Assign clear internal responsibility—who drafts, who reviews for compliance, and who signs on behalf of each party—before beginning recruitment or data collection.
Identify each party by legal name and describe the study scope, locations, and activities covered by the agreement.
State measurable goals, primary endpoints, and the proposed methodology so deliverables and assessment criteria are clear.
Define datasets, de-identification methods, permitted uses, and applicable privacy laws such as FERPA or HIPAA.
Attach participant consent forms and procedures for minors (parental consent and child assent) and describe withdrawal procedures.
Document any participant payments, reimbursements, or institutional compensation and the conditions for payment.
Specify termination rights, indemnity obligations, insurance expectations, and dispute resolution mechanisms.
| Field | Configuration |
|---|---|
| Authentication Method | Email link, SMS code, or stronger KBA for high-sensitivity data. |
| Conditional Fields | Show consent-related prompts only when participant is a minor. |
| Template Reuse | Save a template for recurring studies to reduce drafting errors. |
| Audit Trail Retention | Ensure timestamps, IPs, and signer actions are preserved for compliance. |
Choose a platform that supports required file formats, authentication levels, and secure storage consistent with institutional policy.
Verify platform compliance with institutional requirements (HIPAA BAA if PHI is involved) and confirm long-term access to signed PDFs and audit trails.
Obtain IRB approval before any participant recruitment or data collection begins.
Collect signed consent or assent prior to participation in any study activity.
Follow your IRB or sponsor timeline for reporting adverse events; many require immediate notification.
Meet sponsor or funder milestone dates for interim and final data submissions.
Start renewal or extension negotiations well before the effective date expires to avoid lapses.
Initial agreement assembled and circulated for input from stakeholders.
IRB and legal office review and request revisions as needed.
Authorized representatives and participants sign the final document.
Data collection begins only after executed contract and required approvals are in place.
| signNow | DocuSign | Adobe Sign | PandaDoc | HelloSign | |
|---|---|---|---|---|---|
| Starting Price | $8/user/mo | $15/user/mo | $14/user/mo | $19/user/mo | $15/user/mo |
| Free Trial | 7-day free trial | Varies by plan | Varies by plan | Varies by plan | Varies by plan |
| Bulk Send | Yes | Yes | Yes | Yes | No |
| Audit Trail | Yes | Yes | Yes | Yes | Yes |
| HIPAA Compliant | Yes | Yes | Yes | No | No |
| Envelope Cap | No cap | 100 envelopes/user/year | Varies | Varies | Varies |
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