Grant Writing
Clinical trial protocols aligned to ICH E6(R3), and competitive grant applications built to the funder's template. Fixed scope, fixed price, milestone delivery.
A protocol that will pass ethics review. A grant application that reads like it belongs in front of the funder's reviewers. Both require someone who has written them before and knows the templates and the criteria. For protocols, we deliver an ICH E6(R3)-aligned clinical trial or investigator-initiated study protocol - study design, eligibility, endpoints, a statistical analysis plan outline, and the ethics submission package. For grants, we deliver applications aligned to NIH, ERC, or national and regional funder templates, with specific aims, background, approach, and budget justification. Outline, full draft, revision rounds - each a defined milestone. Book a kickoff call with your target submission and we'll map the timeline.
A protocol that will pass ethics review. A grant application that reads like it belongs in front of the funder's reviewers. Both require someone who has written them before and knows the templates and the criteria. For protocols, we deliver an ICH E6(R3)-aligned clinical trial or investigator-initiated study protocol - study design, eligibility, endpoints, a statistical analysis plan outline, and the ethics submission package. For grants, we deliver applications aligned to NIH, ERC, or national and regional funder templates, with specific aims, background, approach, and budget justification. Outline, full draft, revision rounds - each a defined milestone. Book a kickoff call with your target submission and we'll map the timeline.
Benefit
Written to the template. ICH E6(R3) for protocols. Funder-specific templates for grants.
Milestone delivery. Outline → full draft → revision rounds, with defined dates.
Submission-ready. Ethics package for protocols. Complete application package for grants.
Statistical input included. A statistical analysis plan outline comes with the protocol.
Reviewer-aware. Grants framed against the funder's review criteria, not generic templates.
What's Included
Protocols
ICH E6(R3)-aligned clinical trial or investigator-initiated study protocol.
Study design, eligibility criteria, and endpoints.
Statistical analysis plan outline.
Ethics board submission package.
Grants
Application aligned to the target funder's template (NIH, ERC, national and regional funders).
Specific aims or project summary.
Background and significance.
Approach and methodology.
Budget justification.
On both
Milestone delivery - outline, full draft, revision rounds.
Post-submission support for reviewer queries, on request.
Process
Kickoff call. Study design or funding target, team, and timeline.
Outline. Against the ICH or funder template, delivered for review.
First draft. Full draft against the outline and the supporting data.
Revision rounds. Structured rounds with tracked changes and revision memos.
Statistical / budget input. SAP outline for protocols. Budget justification for grants.
Compliance check. ICH E6(R3) or funder-template compliance review.
Final delivery. Submission-ready document and supporting package.
Post-submission support. Responses to queries or reviewer comments, on request.
Unit of delivery: one protocol or one grant application per engagement. Pricing: fixed price per document type, milestone-based. Turnaround: 3 to 6 weeks for protocols. 3 to 5 weeks for grants from data-ready.
Have a submission on the horizon? Book a kickoff call.
Benefit
Written to the template. ICH E6(R3) for protocols. Funder-specific templates for grants.
Milestone delivery. Outline → full draft → revision rounds, with defined dates.
Submission-ready. Ethics package for protocols. Complete application package for grants.
Statistical input included. A statistical analysis plan outline comes with the protocol.
Reviewer-aware. Grants framed against the funder's review criteria, not generic templates.
What's Included
Protocols
ICH E6(R3)-aligned clinical trial or investigator-initiated study protocol.
Study design, eligibility criteria, and endpoints.
Statistical analysis plan outline.
Ethics board submission package.
Grants
Application aligned to the target funder's template (NIH, ERC, national and regional funders).
Specific aims or project summary.
Background and significance.
Approach and methodology.
Budget justification.
On both
Milestone delivery - outline, full draft, revision rounds.
Post-submission support for reviewer queries, on request.
Process
Kickoff call. Study design or funding target, team, and timeline.
Outline. Against the ICH or funder template, delivered for review.
First draft. Full draft against the outline and the supporting data.
Revision rounds. Structured rounds with tracked changes and revision memos.
Statistical / budget input. SAP outline for protocols. Budget justification for grants.
Compliance check. ICH E6(R3) or funder-template compliance review.
Final delivery. Submission-ready document and supporting package.
Post-submission support. Responses to queries or reviewer comments, on request.
Unit of delivery: one protocol or one grant application per engagement. Pricing: fixed price per document type, milestone-based. Turnaround: 3 to 6 weeks for protocols. 3 to 5 weeks for grants from data-ready.
Have a submission on the horizon? Book a kickoff call.
Question in mind?
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