Beth Lloyd Email & Phone Number

Wilmington, De, Us

Wilmington, Delaware, United States

• Lead governance of Externally Sponsored Research (ESR) proposals and protocols, ensuring strategic review and timely execution.• Develop and communicate ESR strategy for blockbuster brand across functions and to stakeholders.• Manage global portfolio of over 100 ESR studies, driving performance to meet time, cost, and quality standards.• Collaborate with Finance and Supply Chain to manage budget impacts and drug supply demands.• Present performance metrics to Planning and Control committees monthly.• Innovate processes to improve performance, such as leading the IMPACT pillar for research publication metrics.• Support audits, inspections, and regulatory inquiries, acting as a global subject matter expert for ESR agreements.

• Managed US externally sponsored research studies, ensuring adherence to time, quality, and budget.• Coordinated with sponsors and institutions to execute research agreements and regulatory documentation.• Oversaw locally funded ESR studies across five countries, providing mitigation strategies for issues.Document management:• Prepared documents and correspondence.• Collated, distributed, and archived documents (e.g., IRB approvals).• Updated manuals/documents (e.g., SOPs, process guidelines).• Collected proper documentation of destruction of clinical supplies.• Submitted publications for Publication Sign Off using iEnvision platform/CLEAR.

• Negotiated and executed various agreements, including professional service and externally sponsored research agreements.• Managed new supplier setups and reported metrics to leadership quarterly.• Performed Fair Market Value assessment.

• Engaged with senior leadership to define project strategies and objectives and provide leadership for complex, multi-faceted projects spanning multiple functional areas.• Supported alignment of scorecard metrics with the company's strategic objectives.• Served as "Chief of Staff" to VPs, leading business planning and strategy for budget and headcount.• Led a budget simplification project, enhancing efficiencies in planning, monitoring, and reporting.• Developed medical project plans, agendas, and executed large events, leveraging project management skills.• Project managed large multi-workstream PRECISION project to create a new tool to diagnose severe asthma and a technology/digital solution working collaboratively with Medcomms agencies and other suppliers to deliver Ad Boards, Field Communications, Technology Solutions, etc.• Facilitated Congress planning and execution for Medical Affairs.• Planned and organized Core Medical Team meetings, agendas, minutes, speakers, etc.• Managed Medical Affairs annual activity planning, budgets, schedule adherence, resourcing, and milestone reporting.• Actively maintained internal Project Management software (SmartSheet), ensuring consistent accuracy in scheduling, risk assessment, and team data integrity.• Contributed to integrated project teams across a matrixed organization.• Proactively identified and mitigated risks to ensure smooth project progression. • Maintained ongoing communication with key stakeholders to ensure alignment and visibility on project progress and potential challenges.

• Executed HEOR/RWE project contracts, leading local governance review and reporting to senior management.• Streamlined business processes, co-designing governance models and compliance processes.• Developed a HEOR playbook.• Coached, reviewed, and delegated work for team members.

• Sourced activities across professional services, negotiated contracts, and performed spend analysis.• Developed category plans and led supplier negotiations, delivering strategic value to the business.

• Managed spend within the Payer Evidence and RWE sub-category, leading supplier reduction projects.• Developed strategic supplier selection processes, achieving significant cost savings.• Educated business partners on procurement compliance and resolved issues at the project level.

Wilmington, Delaware, United States

• Sourced services for clinical trials, managing contracts and ensuring accurate scopes of work.• Acted as an escalation point for study team issues and managed change orders and discrepancies.• Led a diagnostic tool initiative, presenting final recommendations to the Global Product Team.

• Lead governance of Investigator Initiated Studies for Oncology Product.• Manage high volume of studies to time, cost and quality.• Manage clinical supply shipments to Sponsor sites.• Collect regulatory documentation.

Mba, Management Specialization

B.S., Human Resource Management

Cum Laude

Associate Of Science (A.S.), Business Administration

Certificate, Essentials Of Project Management