Reporting directly to the Chief Clinical Trials Officer, this role is accountable for planning, deployment, management, and oversight of clinical trial delivery operations designed to differentiate Walgreens and its patient experience. Responsible for identifying and deploying compliant Walgreens clinical trial sites, staff resourcing, and ensuring compliance with SOPs to power a tech-enabled clinical trial operating model. -Responsible for the strategy, management (including P&L), and execution of clinical trial delivery operations -Responsible for creating and executing strategy, providing leadership, and day-to-day oversight of all processes, procedures, training, and execution of clinical trials -Accountable for the deployment and implementation of clinical trial sites, resourcing, regulatory and quality control activities -Accountable for clinical site operations, project management, and quality control team members including hiring, onboarding, and training -Accountable for clinical trial budget management and oversight of site payments -Partners with others within Walgreens Clinical Trials leadership to deliver on goals and growth plans -Develops, implements, and executes business plans in support of the attainment of initiatives -Ensures service delivery to all stakeholders, including patients, is of the highest quality and experience -Influences cross functional teams to prioritize and implement capabilities to enable optimal execution -Establishes and reports metrics to determine success of programs, products, etc. -Directs the fiscal and operational analysis resources of the team to forecast the costs and operational impacts of requested changes, training requirements, operational disruption, operational adoption, and deployment timelines and milestones

The Master of Science degree in Clinical Research Administration is an applied program grounded in practical skills to prepare you to lead the business and science of clinical research. Offered through GW’s School of Medicine and Health Sciences, one of the country’s top research medical schools according to U.S. News & World Report, this flexible online program pairs an industry-specific curriculum with accomplished, experienced faculty so that you can have a long and successful career in clinical research administration.

As a HLTH Community Drug Discovery & Development Advisory Board member, I provide insights on relevant content and topics, and regularly lead exclusive virtual roundtable discussions for industry experts and thought leaders to come together and transform healthcare.

The most flexible decentralized clinical trials solution, Curebase’s software and remote-based staff enable participation and data collection from anywhere. As VP of Clinical Operations, I am responsible for oversight of all clinical trial services (i.e., project management, data management, site management and monitoring, virtual site services) to ensure that projects are completed with high quality, on time, on budget, and to the clients’ specifications. As a member of the executive team at a growing startup, I also support numerous activities aimed at improving business operations and establishing our place as a leader in the DCT space.

• Served as primary sponsor representative overseeing outsourced, global clinical trials • Responsible for development and adherence to scope of work (e.g., KPIs, timelines, budget) • Led the RFP process, including vendor identification, evaluation, and selection • Oversaw and contributed to database development and data management activities • Monitored changes to the international regulatory landscape and adjusted plans accordingly • Oversaw the development of patient-facing materials (e.g., consents, study brochures) • Prepared and coordinated scientific meetings (e.g., investigator meetings, conferences) • Developed and maintained risk evaluation and mitigation strategies

• Oversaw site management and monitoring activities for clinical trials and observational studies • Championed initiatives to gain patients’ perspectives regarding lay summaries and consents • Collaborated with data management (e.g., develop CRFs, query tracking, lab data processing) • Served as a change agent driving process improvement for a large network of clinical trials • Facilitate study document creation (e.g., protocol, statistical plan, final report) • Oversaw activities required for trial master file set-up and maintenance • Developed scope of work related to site management and monitoring services

• Led cross-functional teams in the conduct of clinical trials and registry studies • Developed study protocols in collaboration with sponsors and functional group leaders • Identified optimal strategies for engaging with patients throughout the study • Monitored KPIs and presented status to sponsors and management during project meetings • Identified areas of operational inefficiency and facilitated improvements • Contracted with outside vendors and sites, including budget negotiations • Oversaw and contributed to database development and data management activities • Identified issues, conducted root cause analyses, and implemented CAPA plans

• Oversaw project teams conducting large, complex, multi-therapeutic clinical trials • Facilitated teamwork and conflict management among interdisciplinary groups • Developed systems for managing study processes and resources • Oversaw and contributed to database development and data management activities • Led team training activities and contributed to annual performance reviews • Created patient-facing materials (e.g., consents, patient reported outcomes, advertisements) • Led activities for new business including RFP response and bid-defense • Built positive working relationships and confidence with clients to yield new business

• Performed on-site monitoring, co-monitoring, and site management activities • Led monitoring team (i.e., five direct reports) including visit oversight and trip report review • Collaborated with data management (e.g., develop CRFs, query tracking, lab data processing) • Contributed to time and cost estimates for monitoring activities and tracked performance • Authored study plans (e.g., monitoring plan) and informed consent forms • Submitted IRB applications, managed approvals, and released approvals to study sites • Worked directly with site staff to ensure adequate data entry and query management • Contributed to project budget, schedule, and resource planning and management • Developed and actively promoted continuous improvement initiatives

• Oversaw monitoring, regulatory, and site activities for full-service clinical research projects • Worked closely with site investigators and facilitated collaboration among global project team • Performed schedule and budget assessments and tracked performance against baselines • Made significant contributions to clinical study protocol and final study report development • Developed and maintained the project plan, subsidiary plans, and project documents • Worked with data management team to create and support electronic databases • Generated and presented study status reports to client, team, and company executives

• Led multiple studies concurrently and delegated resources to projects with competing priorities • Managed research team members and communicated performance to the site director• Focused heavily on developing and implementing systems for maximizing subject retention • Drafted study specific tools (e.g., source, instruction sheet, enrollment log)• Participated in the review of proposals and facilitated budget and contract negotiations

• Conducted visits with study subjects and performed procedures (e.g., consenting, vitals, ECG) • Handled site regulatory submissions and approvals (e.g., subject materials, amendments, events)• Administered patient reported outcome questionnaires to study subjects• Supervised the collection, processing, and shipment of laboratory samples• Ensured proper storage, handling, dispensing, and reconciliation of investigational products