Who am I?
Hi! I’m Vered Ross, a freelance medical writer specializing in regulatory writing and grant writing for medical device and biotech companies. I have a BSc in Medical Genetics, and was the winner of the British Society for Gene and Cell Therapy 2020 Science Writing Competition.
Here’s a snapshot of my experience:
Grant Writing
Life Science Grant Consultant
Trained by a leading grant consulting agency how to write US federal grants for biotech/medical device companies.
Wrote, optimized, project-managed and submitted SBIR/STTRs (Phase I, Phase II, Fast-track, and Direct-to-Phase II), R01s, R21s, DoD applications, and more.
Regulatory Affairs
Regulatory Medical Writing – Oncology
Worked for almost 3 years as a Regulatory Medical Writer and RA Specialist for an oncology-focused medical device company. I wrote many regulatory documents (clinical study protocols, IBs, IFUs, ICFs, etc.) according to relevant standards (including ICH E6, EU MDR, and medical device specific standards ISO 14155 and FDA CFR 812).
Worked on international submissions, and gained familiarity with working with MHRA, ANSM, FDA, and Health Canada.
Freelance Writer
And now I freelance! I use my combined understanding of clinical trials, regulation, federal grants, and the medical device lifecycle, to help companies draft well-written regulatory documents and grant proposals.
As a reliable and professional freelance writer, I ensure:
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A smooth writing and editing process
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Project management and revisions
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Content with only publication-based or equally reliable evidence
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Compliance with regulations (ICH E6, ISO 14155, EU MDR, FDA CFR 812, etc.).
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An accurately delivered brief
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