I have over 10 years of experience in drug discovery and development across the US, India, and now the UK. As a scientist who transitioned into regulatory medical writing, I bring diverse perspectives from both lab and regulatory environments. This shift has enriched my understanding of the scientific and regulatory landscape. I’m actively driving AI integration into regulatory writing workflows to enhance quality and efficiency. I also share insights on navigating the transition from academia to industry. I hold an IELTS band score of 8.5 (equivalent to C2 level under the CEFR) in English proficiency and B1 level in German proficiency. 📝 Experience in Writing/Reviewing: Academic Publications || Preclinical Study Protocols || Preclinical Study Reports || Clinical Study Protocols || Clinical Study Reports || Narratives || Informed Consent/Assent Forms || Investigator's Brochures || Briefing Books || Administrative Documents ✍🏻 Key Writing Skills: Scientific and Medical Writing || ICH-GCP, CONSORT, ICMJE, and GPP3 guidelines || Drug Metabolism and Pharmacokinetics || Preclinical Research || Phase 1-4 Clinical Development 🔬 Key Laboratory Skills: Immunology || Molecular Biology || Microbiology || LC-MS Bioanalysis || Imaging || In vitro Bioassays 💻 Technical Skills: MS Office || MS Copilot || SharePoint || Veeva Vault || PleaseReview || myClin || EndNote || Clarity PPM || ChemSketch || ImageJ || GraphPad PRISM 🤝 Management Skills: Project Management || Stakeholder Management || KPI/Metrics Reporting || Mentoring and Training ✨ Other Interests: Content Creation || Blogging and Digital Marketing