Isabelle is a highly skilled clinical scientist/clinician with over 20 years of experience in the design, conduct and reporting of Phase 1 through 4 clinical trials across several therapeutic areas, with small molecules, biologics and medical devices. Passionate about data quality, attention to detail, and ensuring scientific integrity of deliverables, she is an independent worker who partners effectively with internal and external stakeholders to deliver quality clinical trials. Her expertise includes study outlines, study design, protocols, informed consent documents, safety narratives, potentially important clinical deviations, safety monitoring, expert review of clinical data and documents, data summarization and clinical study reports. She takes great joy in being part of a team of highly productive individuals coming together to bring better treatments to patients.

When not at work, Isabelle is a passionate birder and bird-photographer, and attends as many of her singer-songwriter daughter’s shows as she can.