RCT Analysis & Systematic Review
Budget: €10,000 – €20,000 EUR
I am coordinating a large-scale healthcare randomised controlled trial and, now that we are midway through data collection, I need an experienced biostatistics partner who can carry the project through to publication and simultaneously prepare a systematic review on the same topic.
For the RCT you will take over live clinical-trial data streams, refine the data collection and management workflow, perform all required statistical analyses, then translate the findings into a clear manuscript-ready report and slide deck. Because the trial is already registered and governed by strict SOPs and GDPR, familiarity with GCP, REDCap (or similar), and reproducible R scripts/SAS code is essential.
Alongside the trial work I also need a full systematic review following PRISMA guidelines. You will handle database searching, screening, risk-of-bias assessment, meta-analysis where appropriate, and prepare a draft that can slot straight into a high–impact journal submission.
Deliverables
• Cleaned, locked master dataset with data dictionary
• Annotated analysis code and statistical output (tables, figures, CONSORT flow)
• Journal-ready RCT results manuscript plus concise presentation deck
• Completed PRISMA flow diagram, evidence tables, and systematic-review manuscript
Please send a formal quote/invoice broken down by milestone so my procurement team can compare at least three offers before moving forward to a short call. Include a brief outline of your relevant trial and review experience, preferred tools, estimated timeline, and any questions you need answered to finalise the quote.
For the RCT you will take over live clinical-trial data streams, refine the data collection and management workflow, perform all required statistical analyses, then translate the findings into a clear manuscript-ready report and slide deck. Because the trial is already registered and governed by strict SOPs and GDPR, familiarity with GCP, REDCap (or similar), and reproducible R scripts/SAS code is essential.
Alongside the trial work I also need a full systematic review following PRISMA guidelines. You will handle database searching, screening, risk-of-bias assessment, meta-analysis where appropriate, and prepare a draft that can slot straight into a high–impact journal submission.
Deliverables
• Cleaned, locked master dataset with data dictionary
• Annotated analysis code and statistical output (tables, figures, CONSORT flow)
• Journal-ready RCT results manuscript plus concise presentation deck
• Completed PRISMA flow diagram, evidence tables, and systematic-review manuscript
Please send a formal quote/invoice broken down by milestone so my procurement team can compare at least three offers before moving forward to a short call. Include a brief outline of your relevant trial and review experience, preferred tools, estimated timeline, and any questions you need answered to finalise the quote.