Linda Miller

Linda Miller is a Senior Clinical Operations Manager with 14 years of experience in clinical research across both animal and human pharmaceutical sectors. She specializes in the end-to-end management of clinical trials, with a strong focus on ensuring studies are executed efficiently, compliantly, and within regulatory and operational standards.

Throughout her career, she has managed the full lifecycle of clinical trial operations, including study startup, protocol development support, clinical trial supply management, vendor oversight, and cross-functional coordination. She is highly experienced in maintaining study timelines and budgets, while ensuring alignment between sponsors, clinical sites, and external partners. Her work also includes active engagement with regulatory authorities to support compliant trial execution and drug development pathways.

In addition to her operational leadership, she contributes to the design and structure of clinical studies, helping shape protocols that support successful research outcomes. She plays a key role in advancing pharmaceutical development by ensuring that clinical trials are conducted with precision and efficiency, ultimately supporting the goal of bringing safe and effective therapies to market.

• University of North Carolina at Greensboro - B.S.
• European Business School at Barcelona - M.S.

• PMP (Project Management Professional)
• CSM (Certified Scrum Master)

• PMI (Project Management Institute)