I’m about to launch an experimental study in the public-health sphere and want a research partner who can take the project from protocol design right through to a publication-ready report. The work starts with refining the research question and crafting a rigorous experimental design that satisfies ethical standards and can pass IRB review. From there, I’ll need a complete data-collection plan, including randomisation procedures, sample-size calculations, and a field-ready set of instruments. If you prefer R, Python, or SPSS for statistical workflows, that flexibility is welcome as long as the analysis plan is reproducible and well-documented. Once data collection is complete, you’ll handle cleaning, statistical testing, visualisation, and interpretation, culminating in a clear results section that aligns with CONSORT guidelines. Finally, we’ll co-author a concise discussion and prepare all tables, figures, and supplementary material so the study is ready for submission to a peer-reviewed journal. Deliverables • Approved experimental protocol with IRB submission packet • Data-collection toolkit (survey forms, codebook, SOP) • Reproducible analysis script and annotated output • Draft manuscript formatted for target journal Completion of each deliverable will be confirmed when the agreed checkpoints (protocol approval, validated dataset, and manuscript sign-off) are met. Let’s produce a study that stands up to scrutiny and advances public health knowledge.