Herbal Ayurveda Clinical Trial Support
Budget: ₹1,500 – ₹12,500 INR
I am moving an Ayurveda-based herbal formulation from concept to human clinical testing and need a research associate who can step straight into both the experimental and analytical sides of the work. The formulation is ready, ethics submission is in progress, and I want a partner to help me finish the clinical trial protocol, oversee data capture, and then run the full statistical analysis once patient recruitment is complete.
The study is a randomized, controlled clinical trial that will compare the herbal intervention with standard care. You will be involved from set-up through final reporting: preparing the SAP, building the REDCap (or similar) eCRF, validating incoming data, running interim looks, and producing publication-ready tables, figures, and confidence intervals in R, SAS, or SPSS—whichever you are most comfortable with.
Deliverables
• A refined clinical-trial protocol aligned with ICH-GCP and Ayurvedic practice guidelines
• A concise Statistical Analysis Plan, including sample-size justification and handling of missing data
• Clean, locked data set with a transparent audit trail
• Full analysis output (code + annotated results) ready for journal submission
• A brief methods-and-results summary to slot directly into the manuscript draft
Acceptance criteria: protocol approved by the IRB, data-quality checks passing 100 % of predefined queries, and reproducible code that regenerates every figure and table without manual edits.
The timeline is flexible but I would like to see the draft SAP within two weeks of project start and first-pass data visualisations by the midpoint of data collection. If you have prior experience with Ayurvedic or herbal-medicine trials, that will be a major plus.
The study is a randomized, controlled clinical trial that will compare the herbal intervention with standard care. You will be involved from set-up through final reporting: preparing the SAP, building the REDCap (or similar) eCRF, validating incoming data, running interim looks, and producing publication-ready tables, figures, and confidence intervals in R, SAS, or SPSS—whichever you are most comfortable with.
Deliverables
• A refined clinical-trial protocol aligned with ICH-GCP and Ayurvedic practice guidelines
• A concise Statistical Analysis Plan, including sample-size justification and handling of missing data
• Clean, locked data set with a transparent audit trail
• Full analysis output (code + annotated results) ready for journal submission
• A brief methods-and-results summary to slot directly into the manuscript draft
Acceptance criteria: protocol approved by the IRB, data-quality checks passing 100 % of predefined queries, and reproducible code that regenerates every figure and table without manual edits.
The timeline is flexible but I would like to see the draft SAP within two weeks of project start and first-pass data visualisations by the midpoint of data collection. If you have prior experience with Ayurvedic or herbal-medicine trials, that will be a major plus.