- Write and edit for science, biomedical, clinical diagnostics, software, nonprofits (especially animal welfare)
- Work at laboratory bench and/or computer to develop, write, and test procedures
- Coordinate writing and publishing process for team of subject matter experts
- Work with clinical and regulatory affairs to develop, revise, and prepare submissions for the FDA
- Conduct interviews, collect data, and write policy documents to meet DOE/NNSA requirements
I offer documentation solutions and technical/professional writing and editing services for a wide variety of business needs. I focus on your audience and provide both your internal and external customers with understandable, usable, and visually appealing materials.
I bring over 20 years of experience in research, field studies, clinical science, diagnostics manufacturing, and project management to writing and editing. My writing experience spans 17 years of technical and professional writing for academic, business, and government environments.
I have started a charitable nonprofit (we received our 501(c)(3) status in March of 2010 [www.greyhome.org]) and bring first-hand experience with animal welfare nonprofits to my writing and editing.
Some client comments:
“Due to your efforts in the generation and revision of technical manuals for regulatory submissions and clinical trials, we were successful in obtaining market clearance... Your positive attitude, rapid response, and dedication in getting the tasks done have made it a pleasure to work with you.”
Celera Diagnostics
From the FDA project lead who reviewed the submission and subsequent response package for a clinical diagnostic that was granted de novo clearance:
“This is actually one of the most well-written responses (for clarity) I’ve encountered. Thanks for the quick response.”
- Style Guides
- User Guides, Quick Start Guides, Quick Reference Cards
- Clinical Trial Training Manuals, Protocols, Reports, Product Inserts and Instructions For Use
- Application Notes / Product Bulletins
- Processes and Procedures
- Presentations
- Science
- Biomedical; Clinical Diagnostics, human and veterinary
- Biotech, High Tech
- Software and computing
- Review raw material, laboratory notes, or other raw content provided by subject matter experts to write and edit for science, biomedical, clinical diagnostics, and software; work at laboratory bench and/or run software on Mac and/or PC computer to develop, write, and test procedures
- Coordinate writing and publishing process for team of subject matter experts and other project contributors; interview internal and external users, gather feedback, and apply to documentation
- Work with clinical and regulatory affairs to develop, revise, and prepare submissions for the FDA; write and edit or revise labeling for clinical diagnostics
- Conduct interviews, collect data, and write policy documents to meet DOE/NNSA requirements
