<div class="content-intro"><p><span style="font-size: 14pt;"><strong>Company introduction:</strong></span></p> <p><span data-ogsc="rgb(0, 0, 0)">Compass Pathways plc (Nasdaq: CMPS) is a biotechnology company dedicated to unlocking urgently needed new treatment options in mental health care. </span></p> <p><span data-ogsc="rgb(0, 0, 0)">The Company is headquartered in London, UK, with a U.S. office in New Jersey. We believe mental health patients deserve the possibility of a better future. Our initial focus is developing COMP360 psilocybin, a proprietary, investigational, synthetic psilocybin treatment under evaluation for treatment-resistant depression (TRD) and post-traumatic stress disorder (PTSD). COMP360 is a potentially first-in-class treatment and has Breakthrough Therapy designation from the U.S. Food and Drug Administration (FDA), as well as Innovative Licensing and Access Pathway (ILAP) designation in the UK for TRD. </span></p> <p><span data-ogsc="rgb(0, 0, 0)">We are leading the world’s largest classic psychedelic clinical program in TRD, and building upon that robust foundation, we are executing a late-stage trial evaluating COMP360 for PTSD, another condition with high unmet need. Our goal is to advance treatments that move the field of psychiatry towards treatment options that offer rapid onset and sustained durability with infrequent dosing. -<span class="Apple-converted-space"> </span><a id="OWA7b9a9bdd-820c-52e3-19e0-7302f475ddce" class="x_OWAAutoLink" href="https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fcompasspathways.com%2F&data=05%7C02%7CAlexis.Rached%40compasspathways.com%7C81c31d1d5b344b36655308deebefbd0f%7Cb94a191dccb54154868e9dcbcb3e1412%7C0%7C0%7C639207612126678649%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=gtzmMKpxYEvhVQspKpFeeyQ6S%2Fq84f%2FpCwFrBs4C4Jc%3D&reserved=0" data-auth="NotApplicable" data-outlook-id="9c215bbc-5d45-4e9b-afdf-92d15cea8a68" data-ogsc=""><u>Compass Pathways</u></a></span></p></div><p><span style="font-size: 14pt;"><strong>Job overview</strong>:<strong> </strong></span></p> <p><span style="font-size: 12pt;">The field-based Health Economics & Outcomes Research (HEOR) Science Liaison is a scientifically trained, field-based expert, that serves as the interface between the company and external healthcare decision makers (HCDMs), including managed care organizations, pharmacy benefit managers, and other health technology assessment bodies.</span></p> <p><span style="font-size: 12pt;">The HEOR Science Liaison delivers credible, non-promotional scientific information across clinical evidence, real-world evidence (RWE), pharmacoeconomic information, and health outcomes to support informed formulary, coverage, and reimbursement decisions. The role spans the full product lifecycle and is key to demonstrating the value of innovative therapies to payer and access stakeholders.</span></p> <p><span style="font-size: 12pt;"><span style="font-size: 14pt;"><strong>Location:</strong></span> Remote in the United States.</span></p> <p><span style="font-size: 12pt;"><span style="font-size: 14pt;"><strong>Reports to:</strong></span><strong> </strong>Director, HEOR.</span></p> <p><span style="font-size: 14pt;"><strong>Roles and responsibilities </strong></span><strong><br></strong><span style="font-size: 12pt;">(<em>Include but are not limited to</em>): </span></p> <p><span style="font-size: 14pt;"><strong>External Scientific Engagement</strong></span></p> <ul> <li style="font-size: 12pt;"><span style="font-size: 12pt;">Identify, cultivate, and maintain peer-to-peer relationships with key payer thought leaders, medical/pharmacy directors, formulary decision makers, Chief Medical Officers, Chief Pharmacy Officers, and other HCDMs within assigned geography</span></li> <li style="font-size: 12pt;"><span style="font-size: 12pt;">Deliver fair-balanced, scientifically rigorous presentations on clinical trial data, real-world evidence, pharmacoeconomic models, and patient-reported outcomes (PROs)</span></li> <li style="font-size: 12pt;"><span style="font-size: 12pt;">Respond to unsolicited medical information requests from payer and access stakeholders with accurate, compliant, and timely scientific content</span></li> <li style="font-size: 12pt;"><span style="font-size: 12pt;">Attend and represent the organization at managed care, payer, and scientific conferences to maintain awareness of current landscape issues and emerging data</span></li> </ul> <p><span style="font-size: 14pt;"><strong>HEOR Evidence Generation & Dissemination</strong></span></p> <ul> <li style="font-size: 12pt;"><span style="font-size: 12pt;">Partner with internal HEOR, RWE, and Medical Affairs teams to identify evidence gaps and support the design, execution, and dissemination of field-based observational studies, retrospective analyses, and pharmacoeconomic research</span></li> <li style="font-size: 12pt;"><span style="font-size: 12pt;">Facilitate investigator-initiated and collaborator-initiated research proposals; coordinate with appropriate internal stakeholders for review and approval</span></li> <li style="font-size: 12pt;"><span style="font-size: