Ramisetty Teja Ramisetty

Medical and scientific writer and PharmD with 4 years of pharmaceutical and CRO experience producing scientifically accurate content across the full spectrum of medical writing, Medical Affairs, and medical communications deliverables. Strong author of manuscripts, abstracts, posters, peer-to-peer slide decks, scientific platforms, congress materials, microsites, monographs, ICH E3-compliant patient narratives, and Clinical Study Reports, with advanced command of GPP3, ICMJE, AMA, and ICH E3/E6 standards. Author of four peer-reviewed publications, including a first-authored review article.

Worked directly on scientific content for dupilumab (Dupixent) and the broader immunology and autoimmune pipeline, with proven ability to immerse quickly in new therapeutic areas. Skilled at clinical data interpretation, statistical results communication, literature review and evidence synthesis, peer review of scientific content, and mentoring junior writers. Recent graduate training in Health Informatics and Digital Product Management adds strengths in digital and AI-supported content workflows.

Comfortable working independently, managing multiple concurrent deliverables, engaging with clients and scientific experts, and collaborating cross-functionally with medical, design, editorial, and agency teams.

Scientific Writer at Sanofi (2022-07 – 2024-08)

Promoted from Associate Scientific Writer (Jul 2022) to Scientific Writer (Dec 2023)

• Authored manuscripts, abstracts, posters, peer-to-peer slide decks, scientific platforms, monographs, microsites, symposia and booth videos, study cards, newsletters, field training materials, and digital content across multiple concurrent deliverables.
• Delivered scientific content across 11+ international congresses including EADV, AAD, WCD, AAAAI, ACAAI, EAACI, CSACI, ATS, and ERS, producing de novo, encore, and adaptation content tailored to each audience.
• Built deep writing expertise in biologics through direct work on dupilumab (Dupixent) and the broader immunology and autoimmune pipeline, partnering with Global Medical Leads to interpret complex clinical trial data and shape clear, accurate scientific narratives for HCP and congress audiences.
• Coordinated publication planning through iEnvision with external writing agencies, tracked timelines and dependencies, and managed citation discipline through EndNote.
• Maintained all content to GPP3, ICMJE, and AMA standards consistently, with strong attention to scientific accuracy, copyright, and citation.
• Conducted regular PubMed literature searches and evidence synthesis, and prepared quarterly literature bulletins to keep medical affairs teams current with emerging evidence.
• Peer-reviewed colleagues' deliverables for scientific accuracy, clarity, grammar, and consistency, and mentored 6 to 7 junior writers on content quality and project execution.
• Recognized multiple times with Bravo and Cheers Awards for scientific accuracy, project quality, and team collaboration.
• Engaged directly with Global Medical Leads, project teams, design, editorial, external agency partners, and stakeholders to solicit input, facilitate alignment, and make content suggestions.
• Served as the central point of contact across the writing team, project management, design, external agency partners, and clients to keep deliverables aligned and on schedule.
• Structured congress content so Regional Medical Affairs teams could readily adapt it for local audiences and specific congress requirements.
• Managed reviews and approvals through Veeva Vault, supporting end-to-end content lifecycle from authoring through final approval.

Medical Writer I at Syneos Health (2021-01 – 2022-07)

• Authored ICH E3-compliant patient narratives at a pace of 4 to 5 per day for Clinical Study Reports, with strong attention to scientific accuracy and consistency.
• Interpreted and wrote from primary references, clinical study protocols, statistical analysis plans, and Clinical Study Reports across multiple therapeutic areas, applying ICH E3, GCP, and ICH E6 standards and FDA and ICH regulations consistently.
• Developed standardized narrative templates that improved team consistency and on-time delivery across concurrent projects.
• Collaborated with biostatistics, clinical operations, and regulatory affairs teams to interpret clinical datasets in Spotfire and ensure narrative accuracy.
• Reviewed clinical data against statistical output to confirm accuracy of in-text tables and figures, supporting overall QC of regulatory deliverables.
• Followed company SOPs, client Working Practices, and client-specific templates and style guides precisely throughout the document lifecycle.
• Managed document projects end to end across drafting, review, consistency checks, QC, and final delivery.

Health Informatics Intern at HouseCall VR (2025-04 – 2025-08)

• Authored an 18-page clinical case study, translating complex healthcare technology into clear medical education content for clinicians and patients in the North American market.
• Developed digital website content for a healthcare platform launch and created infographics, slide decks, and one-pagers for the AWE Conference, all aligned with HIPAA and applicable clinical guidelines.
• Authored post-event reports shared with external stakeholders and produced patient-facing communication content.
• Built hands-on experience with AI-supported content workflows, including Google AI Studio prompt engineering for scientific writing support.

Graduate Certificate in Digital Product Management – George Brown College (2025-09 – 2026-04)

Graduate Certificate in Health Informatics – George Brown College (2024-09 – 2025-08)

Doctor of Pharmacy in PharmD – Nalanda Institute of Pharmaceutical Sciences (2014-10 – 2020-10)