Nicole Rose has over 20 years of experience in clinical research and pharmaceutical operations, specializing in project and program management. She has worked across all phases of clinical trials, including Phase I-IV, registry, non-interventional, and device studies. Her expertise spans global regulatory affairs, clinical trial supply, and data management, with a proven track record in implementing study protocols, feasibility assessments, site activation and oversight, patient enrollment, and quality close-out activities across North America and Europe.

Nicole has contributed significantly to accelerating drug development through the Biopharmaceutical Acceleration Model (BAM), helping shorten the path from lab to life. Her therapeutic area experience includes cardiovascular disease, medical devices, infectious and rare diseases, movement disorders, and ophthalmology indications.

Known for her organized, detail-oriented approach and ability to lead under pressure, Nicole fosters collaborative environments that drive operational excellence and ensure projects are delivered on time and within scope. She earned her bachelor’s degree in chemistry and psychology from La Roche College, providing a strong scientific foundation for her leadership in clinical operations.