Consultation Overview
Research
Proficient in clinical research guidance encompassing protocol development, regulatory submissions, and trial management across all study phases. Experienced in designing ethically sound and scientifically rigorous clinical trials in compliance with Good Clinical Practice (GCP) and regulatory frameworks such as CDSCO. Skilled in site coordination, monitoring, data management, and biostatistical interpretation. Supports investigators in ensuring data integrity, patient safety, and regulatory adherence. Capable of guiding projects from initiation through reporting and publication, contributing to evidence-based healthcare and successful product development.
Service Details
What's Included
- Video consultation
- Personalized guidance and advice
- Session notes and recommendations
- Follow-up support via email
Pricing Options
- Single Session ₹2,000
- Full Project ₹100,000
About Sandeep Thakur
I offer students a blend of academic knowledge and real-world industry exposure, helping bridge the gap between theory and practice through industry-relevant courses, case studies, and hands-on learning. With experience in pre clinical assays, clinical trials and regulatory processes, I mentor students for careers in drug development and research, while building skills in scientific thinking, data analysis, and project management.
Experience
Research Data Analysis
Specialized expertise in research data analysis with 16 years of professional experience.