• Develops and executes company-wide program for delivery of high voltage infrastructure supporting scale data center campus developments. • Serve as a key interface with investor-owned utilities, municipalities and cooperatives, RTO/ISOs, state utility commissions and other regulatory bodies; prepare and oversee filings, testimony and compliance materials. • Lead project portfolio management: scope, schedule, budget, risk mitigation, procurement, contractor oversight, safety procedures and quality assurance for multi-year capital and O&M programs. • Develop and implement asset management, inspection, testing, and emergency response programs specific to substation facilities and equipment. • Ensure compliance with NERC/CIP, FERC, state PSC/PUC requirements and applicable regional transmission planning rules; coordinate reliability studies and outage planning. • Support technical and commercial discussions and contractual negotiations with utilities, ISOs and transmission owners. • Drive continuous improvement initiatives: standardization, cost optimization, digital monitoring (SCADA/telemetry), asset health analytics and lifecycle planning. • Represent the organization in stakeholder meetings, permitting negotiations, landowner and community engagement when required. • Collaborate with Development and Design & Construction teams to provide oversight of high voltage infrastructure facilities construction and commissioning.

• Provides strategic statistical input to and oversees all statistical aspects of assigned programs; • Drives cross-functional collaboration and decision making for program(s); • Oversees the performance of Contract Research Organizations (CROs); • Develop and mentor other statisticians. • Ensures expert level contribution to strategy (design, analysis/synthesis, interpretation and reporting, health authority response, influence and implement publication strategy, quantitative decision making) for critical studies in a program. • Leads collaborations with clinical, regulatory and other strategic functions to drive quantitative decision making and enable successful impact on robust drug development plans. • Maintains indication specific standards with respect to key variables, variable definitions, statistical methods, data structures and presentation of results. • Provides oversight and guidance to staff members within 4DMT and in CROs in completing high quality study deliverables according to agreed timelines following quality standards.

• Primary preparation of statistical analysis plans and expert cardiac safety reports for clients with Clario consulting cardiologists • Provides scientific training to all staff and external consultants • Contribute to the development of a dedicated preclinical-early phase cardiac consulting service for external clients • Supports sponsor meetings (e.g. bid defense meetings, investigator meetings, kick off meetings, teleconferences) originated by project management or business development • Partner with the Sales team to provide sales support as needed • Participate in preparation of regulatory responses and submissions, interactions with health authorities as clinical pharmacology/pharmacometrics subject matter expert (SME) • Responsible for guiding model-based efficacious dose prediction for First-In-Human studies by interpreting and integrating in vitro and in vivo data from nonclinical studies for clients. • Representing Clario at scientific meetings, industry meetings, and webinars • Serve as an internal clinical pharmacology subject matter expert • Travel to client meetings or regulatory meetings may be required • Assist sales with client retention and the development of new clients. • Oversee other contract resources as assigned.

• This position focuses on disease states (e.g. prostate cancer, neuroendocrine tumors, & etc.) being treated by Novartis’ Radioligand Therapies. • The Regional Director of Medical Science Liaisons (RDM) is a field based, non-promotional medical and scientific leadership role. • Their key accountability is the development and execution of an impact-driven medical strategy for their assigned Field Team, aligned with the overarching Medical Strategy, with the goal of improving patient care. • The RDM provides strategic direction and leadership to their assigned Field Medical Team while functioning within the Novartis Code of Conduct, Ethics, Risk and Compliance policies and Working Practice documents. • The RDM drives execution of the medical strategies by setting the direction and providing clear communication of objectives and expectations to Medical Science Liaisons (MSLs) direct reports and strategic guidance regarding key accounts. • They are also accountable for performance of the MSLs within their team, optimal resource management, and the cultivation and recruitment of high performing talent through ongoing coaching and development. • The RDM is responsible for establishing a high performing team culture aligned to Novartis values and behaviors. • The RDM drives cross-functional collaboration through participation in forums to share best practices and build innovation. • They lead cross-functional collaboration with senior internal stakeholders to improve or implement novel approaches to partnerships with external customers (Medical Experts, HCPs, Accounts, etc.) to drive medical and/or clinical goals. • The RDM may serve as a peer leader driving internal initiatives and process improvements for the field teams. • They ensure field training and readiness, scientific expertise, understanding and adoption of technology, and compliant business practices of their respective field teams.