Date of birth : 8 November 1968
Nationality : British
Languages : English (mother tongue), French (fluent)
Specialist in all aspects of the documentation associated with clinical studies, including protocols, informed consent forms, investigator brochures, clinical study reports, Common Technical Document sections 2.5 and 2.7, abstracts, posters/slidekits, and manuscripts for journal submission.
Experience
Medical writing consultant, Lane Medical Writing, Lyon, France
March 2014-present
More than 25 years broad experience of medical writing across all phases of clinical research and including academic, CRO and Big Pharma experience. See www.lane-medical-writing for further details.
Publication manager, Sanofi Pasteur, Lyon, France
December 2008-February 2014
Responsible for publication strategy, planning, and execution for various products and product ranges. Also responsible for coordinating ad hoc non-regulatory documentation and reports to regulatory authorities.
Senior medical writer, Sanofi Pasteur, Marcy l’Etoile, France
November 2004-December 2008
Responsible for writing clinical study reports, protocols, informed consent forms, investigator brochures, and documentation associated with product submissions to regulatory authorities.
Medical writer (Junior-Senior-Team Leader), Covance Clinical Research Unit, Leeds, UK
January 1998-November 2004
Responsible for clinical study reports and publications for Phase I clinical studies (including pharmacokinetic studies: single-dose, multiple-dose, bioequivalence, bioavailability).
Post-doctoral research assistant, University of London, UK
January 1996-December 1997
Responsible for all aspects of a 2-year scientific research project, including writing publications based on the research.
Education
BSc, MPhil, PhD (Physiology), University of Sheffield, UK
1989-December 1996
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