• Develop and execute Enovis’ global clinical evidence strategy supporting pre-market and post-market requirements across FDA, EU MDR, and international regulations. • Define clinical plans to support new product launches, ensuring CEP, CER, PMCFP, and PMCFR are completed on time to prevent revenue delays. • Own the clinical strategy for legacy device remediation under EU MDR to sustain market access and revenue. • Establish global standards for clinical data collection, analysis, and reporting across all business units. • Lead the design, execution, and oversight of clinical investigations, PMCF, PMS, and observational studies. • Partner with internal and external medical writers to develop high-quality clinical evaluation reports, study protocols, CSRs, biocompatibility documentation, and risk management inputs. • Perform gap analyses of clinical data to ensure ongoing certification and compliance. • Review and approve clinical content supporting regulatory submissions and marketing materials. • Oversee clinical monitoring activities at field sites as required. • Ensure compliance with GCP, FDA, ISO 14155, MEDDEV 2.7.1/4, EU MDR, and global regulatory standards. • Function as clinical lead interface with Notified Bodies for product approvals, transfers, deficiency responses, and remediation activities. • Track, manage, and resolve clinical deficiencies, ensuring timely and strategic responses aligned with business priorities. • Maintain readiness for audits and inspections related to clinical documentation and execution. • Collaborate with Regulatory Affairs, Quality, R&D, Medical Affairs, Marketing, and Commercial teams to align clinical evidence with product and business strategies. • Provide clinical regulatory support to global business units. • Represent Clinical Affairs in project team meetings and executive forums. • Identify and develop relationships with Key Opinion Leaders (KOLs) and Centers of Excellence globally. • Lead advisory boards, investigator meetings, and collaborative research partnerships. • Drive clinical evidence dissemination through publications, presentations, and educational initiatives. • Build, lead, and mentor a cohesive global clinical affairs organization. • Own clinical budgeting, vendor management, and resource planning to ensure delivery aligned with business objectives. • Oversee CROs and external vendors for performance, quality, and cost efficiency.

• Ensure world-class study start-up planning and execution by leading teams, strengthening capabilities, and continuously improving how we deliver high-quality clinical trials at speed • Lead and inspire the Study Start-Up Management team • Provide strategic direction and people leadership to SSU Senior Managers • Drive continuous improvement through leadership of the SSU Hub • Oversee SSU operating model performance • Ensure strong SSU management capability through targeted development of skills, processes, systems, and technology expertise • Lead SSU manager resource planning and forecasting • Foster a culture of empowerment, collaboration, and open communication • Build strong partnerships with global and cross-functional stakeholders

• Drive world-class study start-up planning and execution across a global portfolio, ensuring clinical trials launch with quality, efficiency, and speed • Lead and manage a team of Study Start-up Managers, ensuring high-quality, compliant study start-up delivery across multiple programs and therapeutic areas. • Drive end-to-end study start-up planning and execution from global to local, delivering milestones on time, within budget, and in line with ICH-GCP and regulatory requirements. • Provide portfolio-level oversight of study start-up performance, resourcing, and delivery metrics, escalating risks with solution-focused recommendations. • Build team capability through coaching, mentoring, performance management, and role modelling of best practices in study start-up delivery. • Partner with functional and hub leaders to strengthen study start-up capabilities, ways of working, and operational readiness across the organisation. • Own and embed study start-up business processes, ensuring consistent application through training, knowledge sharing, and continuous improvement. • Foster a collaborative, high-engagement culture that encourages innovation, learning, and the sharing of knowledge and best practice. • Contribute to the evolution of the Study Start-up Hub model, shaping future ways of working through feedback, insights, and continuous improvement initiatives.

• Lead deals and opportunities from start to finish • Cultivate, build, and strengthen our relationships with corporate and strategic customers as well as Utility, Muni, Coop customers • Define and execute the market-specific growth strategy by prospecting, relationship building, and identifying clean energy solutions • Prepare RFP and bi-lateral proposals for utility scale solar and energy storage projects. • Negotiate term sheets, MOUs, power purchase agreements, and other commercial agreements with the necessary support and oversight of executive management. • Have a working knowledge of solar and energy storage project development • Understanding ESG goals and activities for Origis as well as for customers • Follow project development activities and maturity for all projects proposed to customers. • Manage vendors and project budgets through SAP system.