Jane has worked in the pharmaceutical industry for more than 25 years within
global pharmaceutical companies and in smaller biotech operations and has developed a broad
knowledge of clinical research and development processes. She has a proven track record of
identifying relational inconsistencies in data and documentation arising within clinical
studies, non-clinical safety pharmacology, pharmacokinetic and toxicology data and within
chemistry, manufacturing and control information.
From 2001, as a co-founder and director of Top Quality Documents she has been
a project leader working with clients managing quality review timelines for multi-document
projects to meet regulatory submission deadlines.
Additional responsibilities within Top Quality Documents include contract
management and collation and analysis of review metrics to support resourcing