Ms. Bulliard has over 25 years’ experience in conducting real-world evidence studies, patient registries, safety surveillance programs, and other specialized real-world programs. She has an extensive global portfolio, specializing in medical device & diagnostics studies.
Ms. Bulliard works with medtech companies around the world to design & deliver solutions that translate evolving methodological real-world research standards and real-world data generation methods into feasible operational delivery strategies to meet the needs of regulators, payers, providers & patients.
A subject matter expert in RWE medical device, diagnostic and digital health studies with a robust knowledge of the current and evolving clinical, regulatory, scientific and commercial medtech landscape, she seeks to generate product value by leveraging the most effective, innovative and compelling strategies within the marketplace.
Ms. Bulliard is a member of IQVIA’s MedTech Center of Excellence representing the domain of real world evidence.
She has previously held senior positions in the field of post market safety and real world research in medical device and biotech companies.
She has obtained her Bachelor of Science in Nursing, BScN, RN, from Dr Steevens Hospital / Trinity College Dublin Ireland, with a P. Grad. Dip in Critical Care ICU Dublin, Ireland and Lausanne, Switzerland.
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