• Accompany Health Med-Psych Associate Medical Directors (AMDs) are key clinical leaders supporting patients and care teams across our Standard and Complex Care models. • You will work with health advocates, physicians, nurses, behavioral health clinicians, and pharmacists to deliver coordinated, whole-person care for patients with complex medical, behavioral, and social needs. • As a Med-Psych AMD, you will clinically supervise Med-Psych and Psych APCs and their care pods in partnership with APC Managers, the Executive Medical Director of Integrated Clinical Services, and BH Managers. • You will also provide virtual mental and physical health care via video, phone, and text. • In the Standard Model, you will lead integrated behavioral health services for patients with mild to moderate mental health and substance use needs, using the evidence-based Collaborative Care Model. • You will act as the psychiatric consultant, supported by Med-Psych APCs and behavioral health clinicians, and collaborate with primary care and APCs to deliver patient-centered, measurement-based, treatment-to-target care. • You will also supervise med-psychiatric APCs providing e-consults for diagnostic clarity and medication management. • In the High-Risk Advanced Behavioral Health Model, you will provide direct and consultative care for a small panel of patients with serious mental illness and/or severe substance use disorders. • You will supervise and support Med-Psychiatric APCs delivering both primary medical and behavioral health care, ensuring multidisciplinary care plans that reduce avoidable utilization and increase patients’ healthy days at home.

• Identifying and maintaining a list of medical/therapeutic area experts, investigator targets and associated plans of action • Establishing, fostering, cultivating and maintaining relationships with KOLs in Hematological Malignancies • Act as the primary clinical/scientific resource for information pertaining to disease state and our products ensuring awareness and understanding • Participates in the development and management of company sponsored clinical trials • Establishing scientific relationships with investigators and internal Medical Affairs, supporting investigator-initiated study (IIS) concept program • Identifying relevant insights on research developments, treatment landscape to shape medical strategy • Identifies gaps in research needs and creates opportunities by collaborating with potential and existing investigators and site personnel • Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific/clinical data • Attend medical conferences collecting and reporting relevant, scientific, clinical, & competitive intelligence • Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally

• Monitor daily clinical quality indicators, trends, and exceptions across all care settings • Ensure adherence to evidence-based clinical standards, policies, workflows, and audit expectations • Provide real-time guidance and escalation support for quality, safety, and workflow concerns • Oversee daily compliance with federal, state, and accreditation requirements (e.g., CMS, state boards) • Lead preparation and readiness efforts for audits; serve as a primary point of contact during reviews • Maintain policies, procedures, and documentation aligned with evolving regulatory standards • Track, investigate, and resolve compliance issues, incidents, and clinical remediation plans • Lead continuous quality improvement initiatives using data, root cause analysis, and best practices • Develop, maintain, and monitor quality dashboards and key metrics • Provide leadership, coaching, and guidance to quality, compliance, and clinical support staff • Support education and training related to quality standards, compliance expectations, and regulatory updates • Communicate quality and compliance performance to executive leadership with clear insights and recommendations • Partner closely with Clinical Operations Audit, Legal, and Compliance to drive aligned and efficient oversight.

• Contribute strategic leadership and medical expertise to the clinical development of our cutting-edge antibody portfolio in rheumatic indications. • Contribute to the study design, execution and interpretation of results, with a focus on proof-of-concept and later phases of development. • Work closely with cross-functional teams including Biostatistics, Regulatory Affairs, and Clinical Operations to support integrated and strategic trial execution. • Provide scientific/medical content and other input as appropriate for INDs, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and other program documents. Ensure compliance with regulatory standards and guidelines, including health authority requirements for MD sign-off on patient-related matters. • Ensure the safety of study participants by actively participating in safety monitoring and data review processes. • Represent the Clinical Development function in interactions with regulatory agencies, investigators, KOLs, and other external stakeholders, as appropriate.