Are you in need of a professional and reliable medical writer? Whether you need a clinical study report written, a NDA or MAA prepared, or a protocol edited, I can help. I can also help with manuscripts for peer-review publications, posters, abstracts, and slide decks.
I am a detail-oriented medical writer who specializes in distilling complex scientific and clinical concepts into comprehensive prose that targets the intended audience: regulatory authorities, C-level executives, stakeholders, clinicians, patients, and/or consumers. I have serves as a key member of medical writing operations in both CRO and pharmaceutical settings. In addition to authoring, reviewing, QC/editing, and publishing regulatory documents across the complete product lifecycle, I also have experience in project planning and management for small and large regulatory submissions.
Services provided include, but are not limited to, the following:
-Preparation of pre-clinical and clinical regulatory documents and dossiers
-High-level literature searches and summary reviews
-Research and preparation of abstracts, manuscripts, and white papers
-Drafting of medical/scientific research news and press releases
-Consumer health communications
-Research and development of science and health articles
-Quality control reviews including data and consistency checks, proofreading, scientific editing, and formatting
