• Designing, planning, coordinating, and conducting all activities involved in initiating, monitoring, and completing clinical research studies in the clinical study sites • Acting as the primary contact and clinical trial expert for assigned study site personnel • Performing site assessments and qualification visits to support the site selection decision process • Developing and managing key study site documentation • Participating in and overseeing CRO delivery of site management activities • Validating product performance claims, supplying data for critical regulatory submissions • Executing site management activities for sponsored studies in assigned focus areas across all phases of study • Working in local and global study teams, including virtual teams

• Support the rollout of new and existing clinical initiatives, policies, standard operating procedures, and best practices across markets. • Coordinate cross-agency projects that enhance care quality, efficiency, and staff engagement. • Partner with agency Directors of Nursing (DONs) and field leaders to ensure consistent understanding and adoption of clinical standards. • Maintain project trackers and dashboards to monitor progress, performance, and compliance milestones. • Assist in identifying opportunities for workflow standardization while respecting local operational differences and regulatory nuances. • Document, update, and maintain standard operating procedures (SOPs) for clinical programs. • Collect and analyze data to inform decisions around staffing models, productivity benchmarks, and program outcomes at the direction of the Head of Clinical Operations. • Support process improvement efforts using quality improvement frameworks. • Partner with the Compliance department to monitor adherence to federal, state and accrediting body regulations (CMS Conditions of Participation, Joint Commission, etc). • Assist in preparing for and responding to internal audits, surveys, and quality reviews and action planning. • Track key clinical quality metrics and assist in creating reports or dashboards for leadership. • Help maintain and disseminate clinical policies, ensuring version control and staff awareness. • Act as a liaison between the corporate clinical operations team and field staff. • Support the planning and facilitation of clinical leadership meetings, training and workshops. • Assist in preparing communications, presentations, and updates for leadership and clinical teams.

• Drive Multi-Project Programs: Lead the end-to-end lifecycle of complex clinical initiatives, collaborating with principal investigators, sponsors, and vendors to execute strategic project plans that meet study objectives • Accelerate Site Activation: Partner closely with research site staff to streamline activation activities and ensure operational readiness for all assigned clinical projects • Design Clinical Frameworks: Collaborate with researchers to develop high-level trial project plans, radiation treatment manuals, and independent review charters to support study design and development • Strategize Funding & Proposals: Lead the development of grant applications and business proposals, coordinating cross-functional input to secure funding and meet critical deliverables • Optimize Matrix Team Performance: Maximize team productivity and work quality by effectively managing resources, balancing competing priorities, and ensuring strict adherence to project timelines • Champion Quality & Compliance: Ensure all clinical activities and documentation maintain rigorous compliance with Good Clinical Practice (GCP) and the Code of Federal Regulations (CFR) • Deliver Executive Insights: Synthesize complex project data into actionable reports for leadership to track progress against organizational goals

• The Executive Director (ED) is the Clinical Operations lead in a country/cluster and is responsible for execution of all Clinical Trials in scope for Global Clinical Trial Operations (GCTO) country operations • Adherence to GCP, local and global policies and procedures to conduct high-quality, inspection ready studies is essential • The position is accountable for trial quality and audit responses and completion of CAPAs • Ensures a single point of contact for managing clinical trial execution in all its aspects across phases in scope of GCTO within the country/cluster • Supports the regional GCTO leadership team, leading strategic development of their country/ cluster to deliver clinical trials as per global clinical research pipeline requirement • Strategic country/ cluster representative for initiatives at all levels of the organization. • Build and lead the team to effectively manage resources ensuring appropriately skilled and high performing team to effectively deliver the portfolio across therapy areas and achieve on agreed GCTO, GCD, and Research and Development objectives