AI Tool for Analysis Plans

Let your AI agent handle the repetitive work of drafting and formatting research analysis plans, so you can focus on study design and results.

You spend hours in Excel, Word, and email rewriting statistical methods and findings for every protocol. As a biostatistician, tailoring each document to fit IRB or sponsor requirements is tedious and error-prone. Manual edits across shared drives and tracked changes drain your time and attention.

An AI agent that drafts, reviews, and formats statistical analysis plans and findings for clinical research, saving biostatisticians hours on documentation.

What this replaces

Rewrite statistical methods in Microsoft Word for each protocol
Copy findings sections from old reports into new templates
Format analysis plans to match journal or sponsor guidelines in Google Docs
Manually update compliance language for IRB submissions
Double-check regulatory terminology in shared drives

The hidden cost

What this is really costing you

In clinical research, biostatisticians often waste 2 hours a week rewriting statistical analysis plans and findings in Microsoft Word, updating regulatory language, and formatting for each protocol. This manual process leads to inconsistencies, missed compliance updates, and delayed submissions. Pulling content from previous reports and adjusting for each study is both monotonous and risky.

Time wasted

2 hrs/week

Every week, burned on work an AI agent handles in minutes.

Money lost

$5,000/year

In salary, missed revenue, and operational drag — annually.

If you keep ignoring it

Ignoring this means higher risk of protocol deviations, delayed IRB approvals, and increased chance of errors in regulatory submissions.

Cost estimates derived from U.S. Bureau of Labor Statistics occupational wage data and O*NET task analysis.

Return on investment

The math speaks for itself

Today — without agent

2 hrs/week

of manual work

$5,000/year/ year

With your AI agent

20 min/week

agent-handled

$833/year/ year

You save

$4,167/year

every year, reinvested into growing your business

Estimates based on U.S. Bureau of Labor Statistics median salary data and O*NET task importance ratings from worker surveys. Time savings assume 80% automation of eligible task components.

Jobs your agent handles

What this agent does for you

Complete jobs, handled end-to-end — so your team focuses on what matters.

Protocol-Specific Analysis Plan

You ask your agent to generate a new analysis plan tailored to a clinical trial protocol.

Methodology Description for Report

You ask your agent to draft a clear, concise description of the analytical methods for a research report.

Findings Summary for Manuscript

You ask your agent to summarize key findings and statistical results for a manuscript section.

Compliance Check for Documentation

You ask your agent to review your analysis plan for regulatory language and formatting before submission.

How to hire your agent

1

Connect your tools

Connect your existing tools, such as data mining, statistical analysis, and document editing software used for research protocols.

2

Tell your agent what you need

Type a prompt like: 'Draft an analysis plan for this phase II oncology trial, including methods, endpoints, and compliance checks.'

3

Agent gets it done

Receive a fully drafted, formatted analysis plan and findings section ready for review or submission.

You doing it vs. your agent doing it

Write each plan from scratch, referencing multiple sources.
Generate a tailored plan with one prompt.
1 hr/week
Reword and adapt previous descriptions for each report.
Receive publication-ready method descriptions instantly.
0.5 hr/week
Manually adjust formatting to match guidelines.
Get documents formatted automatically.
0.3 hr/week
Review and edit language for compliance by hand.
Agent checks and updates compliance language.
0.1 hr/week

Agent skill set

What this agent knows how to do

Draft Protocol-Specific Analysis Plans

Generates comprehensive statistical analysis plans based on your study objectives and uploaded protocol documents.

Summarize Statistical Methods

Writes clear, publication-ready descriptions of analytical techniques for inclusion in clinical trial reports.

Compose Findings Sections

Creates well-structured summaries of key results for manuscripts, using your data outputs from SAS or R.

Review Regulatory Language

Checks and updates documentation to align with ICH-GCP, FDA, or EMA requirements before submission.

Format for Submission

Organizes and formats all sections to fit sponsor or journal templates, ensuring consistent style and structure.

AI Agent FAQ

The AI agent creates analysis plans by analyzing your protocol documents and study objectives. You provide the key details, and the agent drafts tailored sections using current statistical standards. Final review and edits remain your responsibility to ensure alignment with your institution's guidelines.

The agent drafts plans for common statistical approaches like ANCOVA, Cox regression, and mixed models. For highly specialized or novel methodologies, you can add context in your prompt or edit the output for precision.

No raw data is uploaded or stored. The agent processes only the text you provide in your session, and all information is deleted after completion. Data is encrypted in transit using TLS 1.3.

You can specify language preferences, formatting style (e.g., CONSORT, STROBE), and target journal requirements in your prompt. The agent adapts the output, and you can make further edits as needed.

You can copy and paste outputs directly into REDCap, SAS, or R Markdown. Automated integrations are on the roadmap; currently, the agent works with text-based prompts and outputs.

See how much your team could save with AI

Take our free 2-minute automation audit. Get a personalized report showing exactly which tasks AI agents can handle for your team.

Get Your Free Automation Audit

Takes less than 2 minutes. No credit card required.