Alexander Biomedica specializes in producing clearly organized biomedical documentation that coordinates the work of medical experts, researchers and statisticians
in the biomedical sciences.
We draw from a broad knowledge and experience in writing and formatting of biomedical content – from clinical research reports and peer-reviewed publications to supplemental materials, slide kits, and posters for presentation in lectures and biomedical symposia.
We prepare and revise protocols for drug and device trials, including study manuals, informed consent forms, NDA documents, package leaflets, integrated clinical and statistical reports, patient narratives, and clinical expert reports. Alexander Biomedica also writes, edits, and revises manuscripts for national and international scientific journals, monographs, brief communications and abstracts, expert reports and medical textbooks. We also produce topical reviews for medical and scientific websites, integrating text, reference material and graphics for on-line viewing (see our Web Design Page).
- Prepare clinical study protocols, regulatory submissions and clinical reports.
- Summarize data for IND/NDA presentations, as well as FDA submissions and reports.
- Manage on-line submission of manuscripts, grants, and reports.
- Prepare, format, and submit original clinical and basic research manuscripts to peer-review journals.
- Write, edit and format Grant Applications to Federal agencies.
- Organize medical education materials and technical medical content for educational review articles and presentations.
- Literature research summaries
Medical Writing and Non-print media – From inception to final document, integrated software guides your project to completion. MS Word and Endnote citation software ensure accurate and complete literature referencing; data analysis and plotting with MS excel and Sigmaplot graphing software produce professional and accessible graphs and figures. Adobe Illustrator and Photoshop create and refine schematics and photographs. Adobe Pagemaker and Acrobat publishing software produce a final document that brings text, literature citations and footnotes, graphs, and figures together into an easily accessible document.
Background and Experience
- 10+ years experience writing academic/industrial Collaborative Research Agreements (CRAs), including subsequent CRA project management and progress reports.
- 10+ years experience writing, editing, and oversight of Federal Grant Applications to National Institutes of Health, NASA, and US Dept of Defense.
- 10+ years experience coordinating yearly progress reports and renewals in accordance with federal guidelines.
- 10+ years of medical writing in a translational research setting, including proceedings of meetings, original manuscripts, reports, educational reviews, and clinical reference texts.
- 10+ years experience in clinical and basic research data analysis and graphical presentation for a variety of print, presentation and on-line media formats.
- Organized medical education materials and technical medical content in a narrative form for continuing medical education (CME) symposia.
- Excellent working knowledge of medical, pharmaceutical and drug discovery terminology and data presentation.
- Outstanding project management skills.