Associate Director, Evidence Program Management

I am a clinical researcher with nearly 20 years of clinical operations and clinical development experience in both academic and commercial phase I through IV clinical trials. I have successfully worked on trials throughout their life cycle from protocol development through close-out and experience in regulatory inspections. I consider that I am: - a highly motivated, organised and detail oriented person who can work autonomously and within a team to deliver quality outcomes on time and on budget. - an effective director and project manager with experience throughout all stages of clinical trials and across a range of therapeutic areas, including neurology, oncology, cardiology, and endocrinology. - a proven team leader with a high level understanding of the ethical and regulatory framework governing clinical trials within several countries in North America, South America, Europe and the Asia-Pacific region. - excellent at managing the expectations of various stakeholders and communicating across global teams. Please note, I am a Canadian and Australian dual citizen with full working rights in both countries.