Capricor Therapeutics, Inc.

• Develop and execute the territory KOL/HCP engagement plan, including identification, mapping, and prioritization of thought leaders, prescribers and treatment centers.**• Deliver scientific presentations and engage in scientific exchange with KOLs and HCPs on Deramiocel clinical data, the DMD cardiomyopathy landscape, and emerging evidence.**• Support advisory boards, scientific symposia, and KOL-led research initiatives.**• Identify and support investigator-initiated studies (IIS) and real-world evidence opportunities in coordination with HEOR / RWE and Medical Director.**• Provide scientific support for medical congresses, including DMD, neuromuscular, cardiology, and rare-disease forums.**• Collect and synthesize field insights on clinical practice, treatment decision-making, and emerging evidence; translate insights into recommendations for medical strategy.**• Provide scientific training and support to internal stakeholders (Sales, Market Access, Patient Services) in compliance with channel and engagement rules.**• Maintain comprehensive scientific fluency on Deramiocel clinical data, DMD natural history, and the broader treatment landscape.**• Ensure timely reporting of adverse events and product complaints in line with company and regulatory processes.**• Document field activities, KOL/HCP engagement, and insights in Capricor's medical CRM in compliance with standards.**• Ensure all activities follow FDA, OIG, PhRMA Code, ACCME, and Capricor compliance standards.**• Perform other duties as may be assigned from time to time.

• Drive Capricor’s U.S. distribution channel strategy, including 3PL selection and oversight, specialty distributor network design, trade agreements, and product flow from manufacturer to dispensing channel. • Build and run Capricor’s U.S. patient services model across therapeutic areas, including referral intake, benefits investigation, prior authorization, and case management. • Partner with internal teams to support the selection, onboarding, and ongoing management of 3PL, specialty distributor, hub, and specialty pharmacy partners, ensuring clear SLAs, KPIs, and governance frameworks. • Map, standardize, and enhance patient journeys across programs to reduce access friction and support timely initiation of therapy. • Develop and maintain SOPs and training materials for patient and provider facing interactions, ensuring alignment with regulatory, legal, and compliance expectations. • Run financial assistance and affordability programs, including copay, patient assistance, and bridge/quick-start, with external vendors. • Support site onboarding and certification processes for institutionally administered or infused therapies, working closely with treatment centers and operational partners. • Collaborate closely with Market Access to align patient services workflows with payer requirements, reimbursement expectations, and access pathways. • Partner with Commercial Operations and IT to ensure effective data capture, reporting, and system integration across vendor ecosystems. • Develop dashboards, KPIs, and reporting insights to monitor program performance, patient experience, and operational effectiveness. • Define KPIs and build the launch-readiness measurement framework for channel and patient services, covering pre-launch leading indicators and post-launch performance tracking. • Manage relationships and budgets with channel, hub, and patient services vendors; lead RFPs and contracting in partnership with Procurement and Legal. • Build a small team of patient services and channel operations staff over time, and advise Commercial leadership on how the team should grow. • Run ad-hoc analyses and scenario evaluations for Commercial leadership and internal stakeholders. • Establish processes, templates, and tools so channel and patient services execution stays consistent as the company grows.

• Set the vision and roadmap for Commercial Operations in support of Deramiocel's launch, spanning sales operations, analytics, forecasting, incentive compensation, territory design, CRM, and commercial systems. • Build and lead a high-performing Commercial Operations team and operating model tailored to a lean, launch-stage rare disease organization. • Stand up the CRM ecosystem (Veeva or Salesforce), including configuration, targeting, call planning, sample management, and field reporting. • Architect the commercial data environment — data warehouse and aggregator strategy (Databricks, Snowflake), dashboarding (Tableau, Power BI), and integration of claims, specialty pharmacy, HUB, patient services, and distribution data. • Lead forecasting, demand planning, quota setting, territory alignment, and incentive compensation design and administration. • Establish data governance, master data management, and data quality standards across the commercial organization. • Partner with Market Access, Marketing, Medical Affairs, Finance, IT, Legal, and Compliance to align commercial operations with enterprise goals and ensure compliant execution. • Own field force enablement — targeting, segmentation, call planning, field effectiveness analytics, and the operational elements of commercial training. • Design KPI and reporting frameworks that give the Commercial Leadership Team and executive team real-time visibility into launch performance. • Select, contract, and manage commercial operations vendors and service providers, including QBR ownership, SLA oversight, and budget accountability. • Perform other duties as may be assigned from time to time.

• Lead the development and execution of Capricor’s U.S. patient advocacy strategy across therapeutic areas, aligned with pipeline priorities and long term organizational goals. • Identify, establish, and nurture compliant, collaborative partnerships with national and regional patient advocacy organizations. • Serve as a trusted liaison between Capricor and patient communities, fostering consistent, transparent, and ethical engagement. • Integrate patient insights into clinical development, Medical Affairs, Market Access, Patient Services, and Commercial activities to enhance decision making and strategy. • Oversee patient listening initiatives, advisory boards, and insight gathering activities in collaboration with cross functional teams and external partners. • Partner with Medical Affairs and Marketing to develop patient education resources, disease awareness initiatives, and community engagement materials. • Collaborate with Policy, Access, and Patient Services teams, as well as external organizations, to understand and help address systemic barriers affecting patients and caregivers. • Ensure all advocacy activities adhere to legal, regulatory, compliance, and corporate governance requirements. • Track, analyze, and report on advocacy engagement, insights, and program impact to inform future planning and investment. • Represent Capricor at patient focused meetings, advocacy forums, and relevant conferences to strengthen visibility and trusted engagement across communities.

• Develop and execute medical affairs strategies aligned with company goals, including evidence generation, scientific exchange, and medical input into cross-functional teams. • Build and maintain strong relationships with HCPs, KOLs, and patient advocacy organizations in DMD, Becker muscular dystrophy (BMD), and related fields through local, national, and international meetings, 1:1 site visits, and advisory boards. • Collaborate with the CMO to establish high-integrity, compliant processes for HCP and KOL engagement, ensuring adherence to regulatory guidelines (e.g., FDA, ICH). • Create and refine the clinical scientific and value story for deramiocel through internal consultations, external expert input, and data analysis to support program progression. • Lead scientific communications, including publications, congress presentations, and medical information responses, while overseeing vendors as needed. • Provide medical expertise to support commercialization readiness activities, including training, payer interactions, and real-world evidence initiatives. • Work cross-functionally with clinical development, regulatory affairs, commercial, and quality teams to drive business impact and team success. • Identify opportunities for continuous improvement in medical affairs operations, fostering a culture of innovation and compliance. • Monitor emerging scientific data, competitive landscape, and therapeutic trends in neurology, myology, cardiology, and rare diseases to inform strategy. • Perform such other duties as may be assigned from time to time.

• Lead and coordinate statistical related activities to support clinical studies including but not limited to supporting the design, execution, analysis, interpretation, and reporting of clinical trials as well as communication of data evidence. • Support is the statistical aspects of business-critical and/or regulatory commitments, provides input to program plans, and represent the Biostatistics function for cross-functional and intra-departmental teams or working groups. • Functions as the lead statistician for assigned clinical projects. • Performs management of in-house and/or outsourced biostatistical activities. • May engage with regulatory authorities on compound/indication level discussions. • Prepare or review the clinical study protocols, case report forms, statistical analysis plans, and table shells as needed. • Create programs for data management activities, compliant analysis datasets, and statistical analysis of the clinical trial data. • Prepare the statistical section of clinical trial reports and presentations of the results to the team. • Demonstrate solid understanding of regulatory guidance and statistical methodology as applied to clinical studies in pharmaceutical development. • Presenting interim trial data to Data Monitoring Committees (DMCs). • Writing statistical reports and memos with minimal guidance. • Programming complex datasets. • Leading or supporting complex analyses, including efficacy and futility interim analyses for DMCs. • Supports the preparation and documentation of statistical analyses to enable management to write and support trial reports and publications. • Helps ensure that new and revised statistical standards, tests, and processes are implemented for increased accuracy and efficiency. • Reviewing statements of work, proposals, and budgets. • Managing multiple projects and a majority of own workload. • Perform such other duties as may be assigned from time to time.

• Support GCP compliance for clinical operations to ensure regulatory adherence. • Assist in compliance processes and collaborate with cross functional teams to maintain clinical trial integrity.