Ann has worked in Clinical Trials since 2000 across a range of research settings including Primary Care, Secondary care and more recently community based research sites. Ann has experience of trial management and coordination, on-site monitoring in both non-commercial and commercial settings within large multi-site trials and risk-based monitoring systems.
Ann has largely worked in:
She is also interested in Quality Assurance, Research Governance and Project Management of research.
Ann has previously been involved in MHRA Inspections and development of risk-based monitoring and regulatory compliant processes for the sponsorship of CTIMPs. Her work has also included site management, Patient and Public Involvement (PPI) co-ordination, SOP and protocol writing groups.