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Patient recruitment & compliance in clinical trials, Clinical trials operational methodology
MBBS, MBA, PhD, GAICD
Key attributes: strategic thinking, leadership, financial acumen, strong interest in management information systems, pragmatic and strive for efficiency and excellence in the face of major funding constraints.
Wendy is medically trained but has spent her career in clinical trials research, initially in the pharmaceutical industry and subsequently in academic clinical trials research where she has evolved both her research (PhD) and business/management/leadership skills (MBA, GAICD) to complement her clinical insight into specific clinical trial protocols.
Wendy joined the CTC in 1990 as the LIPD Study Manager, the first major phase III cardiovascular study developed and coordinated by the CTC. In 2000 she established the role of Clinical Trials Program Director which she undertook for 18 years, where among other things, she established trial functional teams to support the ever growing trial project teams, oversaw the establishment of electronic data capture, established protocol and budget templates, project plans and standardised reports for metrics and milestones. She did all of this with a major focus on the establishment of major Phase III locally led international trial initiatives.
Wendy is currently the Director of Clinical Trials Strategic Development Initiatives, another new role, which is evolving over time. She is reviewing current CTC systems for finance and trial metrics with a view to standardising reporting across the CTC so data can be shared via a comprehensive organisation dashboard with role/function and program based views.
Wendy also maintains her academic interests via publications, TMC and some external committee membership. Some of her notable publications relating to major/pivotal studies led by the CTC include: