• Work Remotely covering our Central and North Eastern region for our Vascular division. • Comprehensive knowledge in the area of Medical Affairs. • Ability to execute highly complex or specialized projects. • Adapts precedent and may make significant departures from traditional approaches to develop solutions. • Overseeing the direction, planning, execution, clinical trials/research and the data collection activities. • Contributes to implementation of clinical protocols, and facilitates completion of final reports. • Recruits clinical investigators and negotiates study design and costs. • Responsible for directing human clinical trials, phases III & IV for company products under development. • Participates in adverse event reporting and safety responsibilities monitoring. • Monitors adherence to protocols by clinicians within a clinical setting Monitors and determines study completion. • Coordinates and oversees investigator initiations and group studies. • May act as consultant/liaison with other corporations when working under licensing agreements.

• Train operating room staff on Alcon products • Provide on-site and remote clinical support and technical information • Implement equipment and software upgrades at clinical sites • Respond to customer inquiries per standard operating procedures and guidelines • Attend and support medical events and demonstrations • Collaborate with Field Service Engineers and Sales Representatives for installations and support • Provide constant feedback to Research and Development on clinical performance of products via an approved communication plan • Document site visits within 48 hours • Report and address adverse events and device deficiencies, and refer unapproved use inquiries • Achieve required clinical certifications • Advocate for continuous improvement in processes and operational excellence through knowledge sharing

• Travel to customer sites to deliver onsite clinical implementation support, go-live activities, and customer program upgrades for new low to moderately complex customer programs and existing customer upgrades. • Deliver instructor-led education and hands-on product training to clinical staff, super users, and hospital leadership. • Provide onsite coaching, troubleshooting, and end-user guidance to promote confidence and successful adoption of AvaSure solutions. • Collaborate with internal and customer stakeholders to address implementation needs, resolve barriers, and support successful program adoption. • Document implementation activities, clinical observations, and maintain internal records (e.g., hospital data, reports, outcomes). • Maintain current knowledge of AvaSure solutions. • Ensure compliance with credentialing and administrative requirements.

• Plan, implement and monitor study supply strategy overall supply chain strategy in order to maximize efficiency and productivity • Optimize supply levels to ensure continuity while minimizing carrying costs • Control manufacturing and delivery processes • Collaborate with Project Management, Vendor Management, and DLS Leadership • Develop and maintain detailed inventories of study drug • Develop procedures to increase efficiency throughout the supply chain while ensuring quality and safety; implements subsequent changes to processes. • Collaborate with DLS Leadership to define and implement key supply chain KPIs at study and functional levels • Identify process bottleneck and implement solutions in a timely manner • Performs other related duties as assigned.