Role Description Your work will change lives. Including your own. The Impact You’ll Make: Recursion is at the forefront of reimagining drug discovery by integrating automated cell biology, high-dimensional and diverse datasets, and sophisticated analytics. We are seeking a Director-level Clinical Scientist who can oversee all clinical aspects of a clinical trial(s). This would include: - Planning and authoring clinical deliverables (protocols, amendments, medical monitoring plans, annual reports, study-specific updates, CSRs) - Routine medical monitoring - Site interactions/correspondence regarding patient eligibility and treatment inquiries - Presentations, both internal and external As an Associate Director within Clinical Science, you’ll play a critical role in ensuring study protocols are executed appropriately and that the study data is both appropriate and pristine. On a daily basis, you will interact cross-functionally with multiple disciplines supporting the Study Team (Clinical Operations, Medical Director, CMC, Data Management, CROs, CRAs, Investigative Sites, etc). You’ll be responsible for reviewing and cleaning/querying pertinent data points, identifying trends or inconsistencies with the data, and serving as the face of the study to Investigative Sites. You can expect to work on multiple early-phase projects at the same time in a fast-paced and exciting environment where the ability to multi-task and rapidly re-organize thoughts and priorities will be essential. In this role, you will: - Create: Serve as the authoring lead on multiple clinical documents. Recursion is moving away from the use of Medical Writers and relying more heavily on the Clinical Scientist and Medical Director to author IND and study-specific documents. - Collaborate: Work with highly dynamic teams where your role will range from leading and owning decisions or timelines to being a key contributor whose experience and insight are relied upon to advance the task at hand. - Drive & Deliver: You will be primarily responsible for the quality of your study data. This will include reviewing (Medical Monitoring); issuing, reviewing, and closing queries; reviewing TLFs, summarizing data throughout the trial, and presenting the data to management when requested. - Prioritize: Given the nature of Recursion, you will be required to support multiple early-phase (1-2) studies simultaneously. This will require time management and organizational skills. Qualifications - 5-7+ years as a Clinical Scientist in a pharmaceutical or biotech company - Prior experience in early phase 1-2 oncology studies is required - Experience with hematologic malignancies is preferred - Strong interpersonal and communication skills (both spoken and written) - Strong relationship-building skills to work effectively with others in various disciplines and levels - Proven ability to manage multiple, complex, and competing priorities to effective and efficient conclusion - Ability to operate strategically and tactically - Proven ability in problem-solving and issues management that is solution-focused Requirements - This is a fully remote opportunity with occasional travel requirements. - Travel may be necessary from time to time to support collaboration, team events, meetings, or other business needs. Benefits - Estimated annual base salary range for New York City, Boston, & San Francisco Bay Area(s): $234,190–$287,980 - Estimated annual base salary range for Salt Lake City & all other U.S. locations: $212,900–$261,800 - Eligible for an annual bonus, equity compensation, and a comprehensive benefits package. Company Description Recursion (NASDAQ: RXRX) is a clinical-stage TechBio company decoding biology to radically improve lives. Recursion is advancing a portfolio of differentiated investigational medicines across its wholly owned and partnered pipeline in oncology, rare disease, neuroscience, immunology, and other therapeutic areas with significant unmet need. Enabling its mission is the Recursion OS, an AI-native, end-to-end drug discovery and development platform integrating biology, chemistry, and clinical development into a unified intelligence system. Recursion’s platform infrastructure is anchored in Salt Lake City, Utah and Milton Park, Oxfordshire, where its automated biology and chemistry laboratories generate proprietary data at industrial scale. Recursion also maintains offices in New York, Montréal, and London.

• 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.