• Identify, establish, and maintain high‑quality scientific relationships with key opinion leaders (KOLs), investigators, academic medical centers, community physicians, pharmacists, nurses, and treatment centers within the assigned territory. • Serve as a trusted scientific partner by providing fair‑balanced, accurate, and compliant scientific exchange related to disease state, treatment landscape, Kyverna’s CAR‑T programs, and emerging clinical data. • Act as a primary scientific liaison to investigators interested in clinical research collaborations and investigator‑initiated research discussions, in alignment with company policies. • Develop and execute geography‑specific Medical Affairs and KOL engagement plans aligned with therapeutic area objectives, investigator needs, and Kyverna’s medical strategy. • Demonstrate ownership of the assigned territory through stakeholder mapping, prioritization, and proactive planning to influence the patient journey and support optimal therapeutic decision‑making. • Partner with other Kyverna field medical colleagues to share insights and coordinate external engagement approaches where appropriate. • Collaborate with Clinical Development and Clinical Operations colleagues to support Kyverna‑sponsored clinical trials, including: Identification of potential trial sites, Engagement with participating investigators, Support of trial awareness and scientific dialogue, Contribute to efforts aimed at enhancing trial feasibility and enrollment through appropriate scientific engagement with investigators and treatment centers. • Capture and communicate timely, high‑quality medical insights related to the autoimmune and cell therapy landscape to internal stakeholders to support strategy and evidence planning. • Translate external scientific perspectives into actionable insights that inform medical, clinical, and development decision‑making. • Collaborate cross‑functionally with Clinical Development, Clinical Operations, Regulatory Affairs, Commercial, Market Access, and Patient Services teams while maintaining strict non‑promotional boundaries. • Provide scientific support at national, regional, and local congresses, advisory boards, investigator meetings, and medical education forums. • Respond compliantly to unsolicited medical information requests and serve as an internal and external scientific resource. • Maintain current knowledge of therapeutic areas, treatment guidelines, clinical research processes, and cell therapy operational considerations, including treatment center workflows where applicable. • Ensure timely completion of CRM documentation, administrative tasks, required training, and pharmacovigilance responsibilities, including adverse event and product complaint reporting. • Conduct all activities in full compliance with applicable laws, regulations, and company policies.

• Serve as a field-based scientific expert supporting external engagement with healthcare professionals, investigators, treatment centers, and KOLs focused on autoimmune diseases and cell therapy. • Identify, establish, and maintain high‑quality scientific relationships with KOLs, investigators, academic medical centers, community physicians, pharmacists, nurses, and treatment centers within the assigned territory. • Serve as a trusted scientific partner by providing fair‑balanced, accurate, and compliant scientific exchange related to disease state, treatment landscape, Kyverna’s CAR‑T programs, and emerging clinical data. • Act as a primary scientific liaison to investigators interested in clinical research collaborations and investigator‑initiated research discussions. • Develop and execute geography‑specific Medical Affairs and KOL engagement plans aligned with therapeutic area objectives, investigator needs, and Kyverna’s medical strategy. • Demonstrate ownership of the assigned territory through stakeholder mapping, prioritization, and proactive planning. • Collaborate with Clinical Development and Clinical Operations to support Kyverna‑sponsored clinical trials. • Capture and communicate timely, high‑quality medical insights related to the autoimmune and cell therapy landscape to internal stakeholders to support strategy and evidence planning. • Provide scientific support at national, regional, and local congresses, advisory boards, investigator meetings, and medical education forums.

• Identify, establish, and maintain high‑quality scientific relationships with key opinion leaders (KOLs), investigators, academic medical centers, community physicians, pharmacists, nurses, and treatment centers within the assigned territory. • Serve as a trusted scientific partner by providing fair‑balanced, accurate, and compliant scientific exchange related to disease state, treatment landscape, Kyverna’s CAR‑T programs, and emerging clinical data. • Act as a primary scientific liaison to investigators interested in clinical research collaborations and investigator‑initiated research discussions, in alignment with company policies. • Develop and execute geography‑specific Medical Affairs and KOL engagement plans aligned with therapeutic area objectives, investigator needs, and Kyverna’s medical strategy. • Demonstrate ownership of the assigned territory through stakeholder mapping, prioritization, and proactive planning to influence the patient journey and support optimal therapeutic decision‑making. • Partner with other Kyverna field medical colleagues to share insights and coordinate external engagement approaches where appropriate. • Collaborate with Clinical Development and Clinical Operations colleagues to support Kyverna‑sponsored clinical trials, including: Identification of potential trial sites, Engagement with participating investigators, Support of trial awareness and scientific dialogue, Contribute to efforts aimed at enhancing trial feasibility and enrollment through appropriate scientific engagement with investigators and treatment centers. • Capture and communicate timely, high‑quality medical insights related to the autoimmune and cell therapy landscape to internal stakeholders to support strategy and evidence planning. • Translate external scientific perspectives into actionable insights that inform medical, clinical, and development decision‑making. • Collaborate cross‑functionally with Clinical Development, Clinical Operations, Regulatory Affairs, Commercial, Market Access, and Patient Services teams while maintaining strict non‑promotional boundaries. • Provide scientific support at national, regional, and local congresses, advisory boards, investigator meetings, and medical education forums. • Respond compliantly to unsolicited medical information requests and serve as an internal and external scientific resource. • Maintain current knowledge of therapeutic areas, treatment guidelines, clinical research processes, and cell therapy operational considerations, including treatment center workflows where applicable. • Ensure timely completion of CRM documentation, administrative tasks, required training, and pharmacovigilance responsibilities, including adverse event and product complaint reporting. • Conduct all activities in full compliance with applicable laws, regulations, and company policies.

• Individual will work in a team performing functional, relay and SCADA testing in utility level substations. • Equipment acceptance testing, Relay and protection scheme testing, SCADA system testing, troubleshooting and problem solving issues as they arise. • Equipment inspections at vendors facilities. • Individual will have strong communication skills. • Ability to professionally represent the Company with clients, owners, vendors and subcontractors • Push issues to resolution • Self motivated • Excellent ability to understand technical drawings & ability to understand specifications. • Capability and inclination to research and self-teach unfamiliar subject matter. • Perform switching and grounding in energized substations.