Gnyaneswar Ankarboina

Skills

Regulatory & Complianc
-Veeva Vault PromoMats (tagging, annotation, submission, resubmission)
-MLR/regulatory review process management
-Reference pack preparation & source annotation
-AMA Style Guide compliance

Medical Writing & Content
-Scientific slide decks, posters, and abstracts for conferences
-Medical/scientific fact-checking and referencing
-LBLs, VAEs, slide kits, interactive PDFs
-Patient education materials & HCP-facing content
-Medico-marketing content (Oncology, Cardiology, Diabetes, Derma, Immunology, Respiratory)

Research & Data
-Clinical trial data extraction & validation (clinicaltrials.gov)
-Data QC and referencing accuracy checks

Project & Team
-Multi-project management under conference deadlines
-Junior writer mentoring and QC review

Tools
-Veeva Vault, Power BI Desktop, Advanced Excel, Microsoft Office, Regeneron

About

Medical fact-checker and scientific writer with 8+ years of experience spanning drug safety, medical/scientific writing, and medical data fact-checking. Currently fact-checking and referencing scientific claims for materials presented at major international conferences (EADV, ESDR, EULAR, Gene to Clinic) and managing end-to-end MLR submissions via Veeva Vault PromoMats — from tagging and annotation to final compliant submission and resubmission. Prior experience includes annotating client-approved digital assets against source documents, preparing reference packs, and resolving MLR comments as an Associate Scientific Writer, plus medical content writing for patient- and HCP-facing materials. Comfortable managing multiple concurrent projects under tight, conference-driven deadlines across Immunology (Dermatology/Rheumatology/Gastroenterology), Oncology, and Pulmonary Arterial Hypertension. PharmD-qualified, India-based, available remotely.