• Responsible for the end-to-end lifecycle of our PAM services • Design and implementation of CyberArk solutions • Ongoing maintenance and support of our CyberArk environment

• Apply specialized, clinical knowledge to hospital partners: categorize, code, summarize, interpret and calculate registry/case information from nuanced, patient medical records. • Ensure quality submission of all data in specified registries or measure data repositories, maintaining a high accuracy threshold. • Prioritize, organize, and meet tight deadlines for multiple concurrent tasks and team requests; uses tact and judgement to manage expectations, flag obstacles and propose solutions in a timely manner. • Navigate new technical systems: electronic medical records (EMR) and registry/case entry tools; use team resources to troubleshoot technical issues with systems and applications with a focus on solutions. • Contribute to team best practices, data dictionaries, abstraction guidelines, and other business rule documents; identifies process improvement opportunities to help streamline tasks and processes. • Keeps up to date on mandated regulatory/publicly reported data requirements as specified by federal, state, payer and other agencies. • Any or other additional responsibilities as assigned

• Lead full-cycle recruitment processes • Develop creative and effective sourcing strategies • Conduct interviews and assess candidates • Maintain strong relationships with clients and candidates

• Become a SMA and apitegromab medical/clinical/scientific expert • Build and foster relationships with local, regional, and national KOLs and possibly Payers • Effectively deliver medical/clinical/scientific presentations to a diverse external audience • Support clinical development activities, investigator recruitment and education • Development and execution of their Territory Management Plan (TMP) that is aligned with the overall Medical Goals and Plan • Contribute to developing metrics, qualitative and quantitative MSL reports, SOPs/Business Practices for the MSL function • Responding to unsolicited medical information requests submitted by SRRK field teams (eg. Sales and Market Access) • Compliantly partner with Sales and Market Access on high-level regional engagement • Provide internal teams with insights from interactions and discussions with HCPs • Co-create and deliver the MSL training • Provide content development support for MSL materials, alongside the Director of Medical Communications • Contribute to the development of the Global and US Medical Plans for apitegromab in SMA • May be asked to participate in Advisory Board meeting, Advisory Group meetings, speaker trainings, etc. • Coordinate local and regional investigator-initiated research (IIR) • Compliantly manage IIR milestones and objectives • Report on scientific sessions and conduct scientific exchange to unsolicited questions at SRRK medical booths at congresses • May respond to and document unsolicited requests for scientific information • Conduct all activities and responsibilities in accordance with all relevant legal, regulatory and corporate regulations and guidelines, including the Scholar Rock Business Conduct & Ethics, policies and procedures