Alisha Reader

Background

About Alisha Reader

Clinical drug development professional with 17 years of clinical research industry experience in both small biotech and large pharma. Operations leader, with expertise in global cross-functional clinical operations and strategy. Passion for development of high performing leaders and cohesive teams. Key expertise in directing global clinical development portfolios with multiple assets, team development, resource allocation and utilization, performance and quality indices, risk mitigation strategies, financial forecasting, and driving successful project teams. Extensive vendor management experience, including qualification and selection, contracting, and governance. Exceptional relationship builder. Keen interest in cross-functional process improvements and standardization, developing efficiencies and cost-effective solutions to business challenges. Subject Matter Expert (SME) in clinical trial systems and applications (i.e, CTMS, EDC, eTMF), including evaluation, selection, development and systems validation.