Statistical Help for Clinical Research
Rigorous Analysis for Your Clinical Trials and Studies
From protocol development to final manuscript, robust statistical analysis is critical for the success of your clinical research. At Thesis Writing Cafe, our team of biostatisticians provides expert statistical help, ensuring your study is well-designed, your data is accurately analyzed, and your findings are ready for publication and regulatory submission.
PhD-Level Biostatisticians
ICH-GCP Compliant
Publication-Focused
Our Clinical Research Statistical Services
Why Choose Our Clinical Research Statisticians?
Industry & Academic Experience
Our team has extensive experience in both academic medical centers and the pharmaceutical industry.
Regulatory Knowledge
We are well-versed in the statistical requirements of regulatory bodies like the FDA, EMA, and CDSCO.
Collaborative Approach
We work as a seamless extension of your research team, collaborating closely with PIs, CROs, and sponsors.
Focus on Clear Communication
We translate complex statistical output into clear, understandable results that support your study’s conclusions.
Data Integrity
We follow strict procedures for data handling and analysis to ensure the integrity and reproducibility of your results.
End-to-End Support
From the initial grant proposal to the final publication, we provide comprehensive statistical support.
Our 4-Step Process
Submit Requirement
Share your research area and specific needs through our consultation form.
Get Quote & Plan
Receive a customized plan and a detailed quote for your project.
Collaborate with Expert
Engage in one-on-one sessions with your dedicated academic mentor.
Receive & Review
Get your completed chapters, provide feedback, and request revisions.
Our Authoritativeness & Recognition
Thesis Writing Cafe is a registered and verified business, recognized on major international platforms for our commitment to quality.
Frequently Asked Questions
What stages of clinical research do you provide statistical help for?
We provide end-to-end statistical support for all stages of clinical research, including protocol development, study design (Phase I-IV), sample size calculation, Statistical Analysis Plan (SAP) development, data analysis, and manuscript preparation for publication.
Are your services compliant with regulatory standards like ICH-GCP?
Yes, our team of biostatisticians is well-versed in the statistical requirements of regulatory bodies, including ICH-GCP, FDA, and EMA guidelines, ensuring your research is compliant and ready for submission.
Can you help with the statistical section of a grant proposal for clinical research?
Absolutely. We specialize in developing robust statistical analysis plans for grant proposals to funding agencies like the NIH and ICMR, which can significantly increase your chances of securing funding.
What Clinical Researchers Say
“The statistical expertise provided for our Phase III trial was exceptional. The analysis was robust, and the SAP was developed flawlessly. They are a reliable partner for any clinical research team.”
“Their review of our manuscript’s statistical section was meticulous. They caught a critical error and helped us present our findings more accurately, which was key to our publication in a high-impact journal.”
“As a CRO, we need partners we can trust. Thesis Writing Cafe consistently delivers high-quality, timely, and compliant statistical analysis for our clients’ projects. They are our go-to for biostatistics.”
Our Location
Ready to Enhance Your Clinical Research?
Ensure your study’s statistical integrity and impact. Contact us for a free, confidential consultation with a clinical research statistics expert.