Experienced medical writer specialized in regulatory writing. Have good knowledge on documentation of drug information queries, non clinical and clinical documents/reports, and regulatory documents/reports. Have good knowledge and experience in the area of clinical research for development of Plain Language Summaries, Informed Consent Forms, PADERs, PAERs, Patient Narratives, and posting of disclosure documents in the area of regulated and policy driven clinical disclosures and data sharing for public disclosure registries.