Starting her career as a CRA, progressing to Project Manager and Medical Writer, Wendy Kingdom has experience of writing all study-related documents from
study conception to completion
Protocols
Clinical Study Reports
Information for Patients Leaflets and Consent Forms
Other patient information such as instructions for using medication, and appointment cards
Regulatory summary documents, including clinical summaries and overviews, PIPs, ODDs, clinical expert statements for product license renewals, and editing of scientific advice documents
Ethics Committee applications
Safety narratives
SOPs
Manuscripts for publication