About This Project

You're a researcher in the early stages of trial development. Maybe you just have an idea, or maybe you have a protocol. From "what if" to IRB approval and your first enrollment, I provide guidance and help you develop your protocol, informed consent, recruitment materials, and trial design. My advanced ICH GCP certification ensures that your study meets the highest standards for regulatory requirements, research participant protection, and research ethics. Compare available packages below.
Basic
Project Review and Editing
Your trial has been designed: you have developed most documents, but may need assistance developing more (e.g., you have a protocol but not an ICF or recruitment materials). Includes proofreading and editing of existing documents, addition of up to 5,000 words, and style guide formatting if required. ✔ Proofreading & editing✓ Additional research✓ References & citations✔ Style guide formatted 🕒 14-day delivery 📄 5000 words included ⚡ 10 days (+$200) ⭮ 2 revisions
$935 USD
Standard
Concept Enhancement
Your trial is roughly 50% developed. You have developed some documents, but they are incomplete. Includes proofreading and editing of existing materials, additional research if required, up to 8,000 extra words, and style guide formatting when applicable. ✔ Proofreading & editing✔ Additional research✓ References & citations✔ Style guide formatted 🕒 21-day delivery 📄 8000 words included ⚡ 15 days ($395) ⭮ 2 revisions
$1,585 USD
Premium
Trial Design and Development
You have an idea and potentially some loose documentation or framework in place, but need help designing your trial. Includes protocol development, ICF, etc. Please note this does not include statistical consultation, including assessment of study power or development of an SAP. Research support is provided, as well as up to 16,000 words. ✔ Proofreading & editing✔ Additional research✔ References & citations✔ Style guide formatted 🕒 30-day delivery 📄 16,000 words included ⚡ 21 days (+$590) ⭮ 3 revisions
$2,175 USD
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