• Provide clinical development leadership to one or more programs. • Contribute to clinical development strategy in alignment with enterprise goals and management. • Serve as medical monitor for one or more studies. • Perform ongoing clinical trial data review and cleaning in collaboration with clinical science and pharmacovigilance. • Attend and contribute to study team meetings. • Present clinical trial findings to management. • Author clinical documents (protocol, investigator brochure). • Author clinical portions of regulatory documents (IND, CTA, NDA, MAA or equivalent). • Develop and manage relationships with key opinion leaders for clinical programs. • Organize, manage and lead Steering Committees and contribute to Strategic or Clinical Advisory Boards. • Contribute to writing of manuscripts, publications, or other documents intended for external audiences. • Contribute in an active and ongoing manner to the scientific, clinical, and commercial development of current and future product candidates. • Contribute to company culture and growth. • Foster communication, collaboration and coordination with other functions. • Contribute to maximizing synergistic collaboration between Ono and Deciphera. • Contribute to assessment of new internal or external targets by outlining clinical challenges and opportunities. • Support Medical Affairs activities as needed. • Participate in and/or coordinate cross-functional continuous improvement projects. • Act as an internal resource for functions requiring clinical input on select drug(s) including primary point of contact for clinical trial staff at study sites for clinical issues as well as regulatory, safety and other functions.

• Provide clinical oversight and supervision for provider teams including psychiatric nurse practitioners and therapists. • Develop and implement evidence-based treatment protocols evaluating impact on patient outcomes and revenue sustainability. • Build and oversee quality assurance to ensure adherence to clinical best practices, safety standards, and regulatory compliance. • Provide clinical supervision and mentorship for psychiatric nurse practitioners, conducting case reviews and supporting direct patient care. • Lead the clinical strategy and vision for women's reproductive mental health services. • Partner closely with executive leadership to shape the strategic direction of FamilyWell by providing clinical expertise that drives the development and expansion of innovative service offerings and clinical programs. • Analyze data and clinical outcomes to develop insights for clinical practice and presentation of thought leadership both internally and externally. • Stay current with emerging research and integrate new findings into clinical practice. • Participate in product development and clinical innovation initiatives.

• Serve as a senior clinical leader and addiction medicine subject matter expert across the organization. • Partner with Clinical Services leadership to strengthen clinical quality, consistency, and patient safety across Boulder’s care delivery model. • Lead routine review and refinement of clinical protocols, formulary standards, and evidence-based practice guidelines. • Support quality assurance activities, chart review processes, and clinical audits to identify opportunities for improvement. • Provide consultation and guidance on complex clinical cases and emerging clinical issues. • Ensure Boulder’s clinical standards remain aligned with current evidence, regulatory requirements, and payer expectations. • Partner with Clinical Services leadership to strengthen clinical leadership capabilities across the organization. • Provide mentorship, coaching, and support to clinical leaders and clinicians navigating complex clinical and operational challenges. • Help establish and reinforce standards of clinical excellence, professional growth, and evidence-based practice. • Contribute physician leadership and oversight to clinician education, onboarding standards, and ongoing clinical development programs. • Support the development of systems that promote accountability, consistency, and continuous improvement across the clinical organization. • Translate quality findings, operational priorities, and emerging evidence into scalable clinical workflows and care delivery standards. • Identify gaps in clinical processes, policies, and infrastructure and partner across teams to implement solutions. • Support implementation of new clinical initiatives and ensure clinical best practices are operationally viable and consistently applied. • Drive adoption of new clinical workflows, protocols, and care models across a distributed clinical workforce. • Partner with Medical Affairs and Clinical Services leadership to evaluate and support expansion into new service lines and care models. • Assess clinical readiness, staffing considerations, protocol requirements, and quality implications for new programs. • Ensure new services are designed with appropriate clinical governance, quality standards, and outcome measurement strategies. • Contribute clinical expertise to Boulder’s long-term vision of comprehensive substance use disorder care. • Serve as a clinical liaison to Product, Operations, Analytics, and other cross-functional teams. • Translate clinical priorities into product requirements, workflows, and operational processes. • Provide clinical input on care delivery technology, clinical decision support tools, AI-enabled workflows, and platform enhancements. • Ensure operational and product changes are evaluated through the lens of patient safety, clinician experience, clinical effectiveness, and quality.

• Lead the end-to-end internal and external medical communications that support the product portfolio. • Accountable and responsible for all aspects of scientific and medical information, education, and communication for Freenome’s cancer screening portfolio. • Manage medical communication agencies and foster cross-functional partnerships to maintain a consistent medical voice. • Own the end-to-end Medical Information Inquiry response process from intake through resolution. • Develop and update Freenome's medical content including FAQs, slide decks, and training materials. • Support the development and delivery of Medical Communication activities including scientific communications platforms. • Collaborate across Medical Affairs, Marketing and Sales Training on claims matrices to ensure alignment of materials. • Manage scientific communications platforms and medical communications agency partners.