eSupervisor Detail

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.)

WHO IS THIS FOR? Pharmacy, medicine, or life sciences students and researchers who need help drafting, editing, or structuring research articles, case reports, review articles, conference abstracts, or scientific posters. WHAT YOU GET With 2 peer-reviewed publications in international journals (JPRI 2024, WJPR 2023) and advanced certification in Medical Writing, I help you communicate your research clearly and compellingly — in a format that editors and reviewers actually want to read. DELIVERABLES • Research article drafting or editing (introduction to discussion) • Case report writing (history, investigations, management, discussion) • Literature review and background section writing • Abstract writing for journals or conferences (structured/unstructured) • Scientific poster design content (text, layout guidance)• Proofreading, language editing and journal formatting