Telephone +1 (609) 631 0990
Email fjones170901@optonline.net

Would you like to issue a company newsletter but don't have the time?

Do you need scientific content to keep your website up-to-date?

Are you snowed under with clinical trial reports?

Email me

• Experienced writer providing on-line and traditional print media to pharmaceutical/biotechnology companies and related industries including CROs and scientific recruitment agencies.
• A flexible, cost-effective solution for your medical writing needs.
• Quality, accuracy and confidentiality assured.
• Documents prepared in accordance with appropriate style and regulatory guide, e.g. AMA, ICH, MLA, The Chicago Manual of Style etc.

   

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• Website content e.g. Honeycomb Connect Compliance Column
• Study protocols, clinical trial reports, investigator brochures, safety summaries and SOPs prepared all in accordance with the latest regulatory guidelines.
• Meeting reports.
• Pharmaceutical/biotechnology newsletters and ezines edited and uploaded directly to your site or emailed to your subscribers.
• Articles written for pharmaceutical/biotechnology industry magazines e.g. GCPj and BTi.
• Advise and develop company publicity documents and websites e.g. OneScience
• eBook preparation.
• Manuscripts written for scientific journal submission.

• Pharmaceutical professional with experience of working in a multi-national and multi-disciplinary environment.
• Broad portfolio of published articles.
• 10 years freelance experience supported by full-time positions in the pharmaceutical industry and the British National Health Service.
• Skilled at presenting complex data in a clear and concise manner.
• Extensive knowledge of the entire clinical trial process from conception through to registration.
• Read my Published Works and  Full Resume

Biography

Friendly colleagues suggested that she might be better suited to a desk-based job when she kept correcting their reports and rewriting the procedure books. Heeding this advice, she joined the Regulatory Affairs Department of SmithKline Beecham (now GlaxoSmithKline) in Weybridge, Surrey and her writing career was launched.

Ms. Jones gained first-hand knowledge of the regulatory data she had prepared when she became a Clinical Research Associate for the company. This career transition has given Fiona a broad understanding of the entire clinical trial process, with a unique perspective on the complexities of regulatory compliance.

In 1994, Fiona realized the potential for balancing work and leisure time and started a freelance-medical-writing business. Although initially based in England, the beauty of the French countryside beckoned and in 1996, Ms. Jones (and her freelance writing) moved to Burgundy. The travel-bug got the better of Fiona again in 2000 when she crossed the Atlantic and settled in New Jersey, U.S.

Managing  Editor for OneScience 

Contributing Editor for Honeycomb Connect   

Freelance Writer for Novartis Pathways