2010 - maintenantWriting clinical and regulatory documents (including study protocols, informed consent forms, investigator brochures, reports and publications) for the pharmaceutical industry.
Marly-le-Roi 2005 - 2010Responsible for writing a broad range of clinical and regulatory documents for both prophylactic and therapeutic cancer vaccines. Co-ordinated the document preparation activities of teams of science writers and lead a multi-disciplinary taskforce on informed consent.
