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 FIONA JONES
Phone: +1 (609) 716
1534
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SUMMARY |
Medical writer with extensive portfolio of
published articles.
Broad knowledge of the entire clinical trial process from
conception through to registration.
Experienced with a wide selection of media - scientific
journals, clinical trial documentation, eBooks, on-line
newsletters (ezines) and websites.
Ability to work independently to tight deadlines.
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ON-GOING PROJECTS |
Managing Editor for
OneScience
Contributing Editor for
Honeycomb Connect |
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CAREER HISTORY |
Freelance Medical Writer - 1994 to
date
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Clients: ADIS International (New
Zealand), Biotrial (France), Brookwood Medical Publications
(UK), Elsevier Publications (Belgium), Groupe Fournier
(France), Honeycomb Connect (Canada), Inlingua (France),
Oncodesign Biotechnology (France), OneScience (USA),
Pharmajobs (Germany) and Glaxo SmithKline (UK).
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Services: Write/rewrite manuscripts
for journal submission.
Edit and distribute pharmaceutical/biotechnology newsletters
and ezines.
Prepare study protocols, clinical trial reports,
investigator brochures, safety summaries and technical
documentation including standard operating procedures
(SOPs).
Provide training in the preparation and use of prepared
documentation.
Identify, evaluate, contact and meet potential
collaborators.
Prepare and maintain strategic databases of clients and
competitors.
Advise and develop company publicity documents and websites.
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1989 - 1994
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Glaxo SmithKline, Consumer
Healthcare, Surrey, England.
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1994 |
Regulatory Compliance Associate (3 month
secondment) - Introduced a computerize project planning
system to establish, promote
and monitor the progression of GCP/GLP/GMP.
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1992 |
Senior Clinical Research Associate (Oral
Health) - Coordinated clinical trials: worked with external
consultants and Contract Research Organisations (CROs) to
design protocols and conduct studies, monitored trials,
prepared reports and presented results to senior management.
Audited CROs, study sites and internal procedures to GCP.
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1989 |
Regulatory Affairs Executive (OTC Medicines,
Oral Health) - Compiled registration dossiers to licence
pharmaceutical products within Europe. Liaised with
technical colleagues, suppliers and manufacturing sites to
define and request data necessary to respond to queries
received from regulatory authorities. Specific
responsibility for TUMS, Macleans and Aquafresh.
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1987 - 1989
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Queen Mary's University Hospital,
London, England.
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Medical Laboratory Scientific Officer -
Performed routine biochemical analysis and analytical
development.
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1986 - 1987 |
Birmingham & Midland Hospital
for Women, Birmingham, England.
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Junior Medical Laboratory Scientific Officer
-Performed endocrine function tests by radioimmunoassay.
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EDUCATION |
Institute for Business and Professional Development, Mercer
County College, Trenton, New Jersey, USA.
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2002 - 2003 |
Business and Marketing Writing
Introduction to networking
Marketing your business or organization on the internet
Creating eBooks
Creating Web Graphics with Paint Shop Pro
Advanced Web Pages (HTML)
Creating Web Pages with HTML
Introduction to PC Troubleshooting
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1983 - 1986 |
Aston University in Birmingham.
England.
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B.Sc. Combined Honors PHARMACOLOGY &
BIOCHEMISTRY
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PROFESSIONAL MEMBERSHIP |
British Institute
of Research Quality Assurance (BARQA)
European Medical Writer's Association (EMWA)
American Medical Writer's Association (AMWA)
Registered with URSAFF de la Cote d'Or, France 1998
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ADDITIONAL INFORMATION
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Nationality:
Irish
Date of birth: 26 October 1964.
Basic understanding of spoken and written French.
Fully conversant with an extensive range of computer
software.
Interests include digital photography and genealogical
research.
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