Consultation Overview
Clinical Research Guidance
WHO IS THIS FOR? Pharmacy/life sciences students, junior CRAs, CRCs, or early-career professionals who need hands-on guidance on clinical trial processes, eTMF compliance, pharmacovigilance, or regulatory frameworks.
WHAT YOU GET Drawing on 8 months of industry experience at IQVIA, one of the world's largest CROs, I guide you through real-world clinical research workflows: from GCP principles and eTMF document management to PV reporting and regulatory compliance, giving you the practical edge that textbooks don't.
DELIVERABLES • 1-on-1 mentoring session on clinical trial phases, GCP & ICH guidelines • eTMF / TMF structure walkthrough (Veeva Vault, document lifecycle) • Pharmacovigilance basics: AE/ADR/SAE/ICSR reporting explained • Career roadmap for breaking into CROs / pharma companies • Study design guidance (RCT, observational, prospective/retrospective) • Personalised resource list and study plan for certifications (ICH-GCP, etc.)
Service Details
What's Included
- Video consultation
- Personalized guidance and advice
- Session notes and recommendations
- Follow-up support via email
Pricing Options
- Single Session ₹1,000
- Full Project ₹8,000
About Sameera Shabnam
Clinical research–oriented PharmD graduate with strong knowledge in pharmacology, clinical trials, and data analysis. Skilled in literature review, protocol understanding, and patient-centric research approaches. Passionate about mentoring students in clinical research, pharmacovigilance, and evidence-based practice while helping them build practical, industry-relevant skills.
Experience
Research Data Analysis
Specialized expertise in research data analysis with 1 years of professional experience.