Recursion

Medical Director

• Lead clinical pharmacology and pharmacometrics strategy and execution for rare disease and oncology clinical programs
• Develop clinical pharmacology and pharmacometric strategies supporting product development plans
• Serve as Clinical Pharmacology lead for clinical development programs and representative for regulatory interactions
• Perform and/or oversee modeling and simulation to solve drug development questions and expedite decision-making
• Provide clinical pharmacology input on Phase 1–3 clinical studies and dedicated Phase 1 clinical pharmacology studies
• Author and review clinical pharmacology sections of Investigator’s Brochures, INDs, NDAs, and other regulatory submissions
• Act as clinical pharmacology expert during health authority interactions
• Collaborate with clinical study, translational, preclinical, and due diligence teams
• Work within Recursion’s Pharmacometrics team across Discovery and Development projects

Executive Director, Clinical Pharmacology/Pharmacometrics

• Lead clinical pharmacology and pharmacometrics strategy and execution for rare disease and oncology clinical programs
• Develop strategies supporting product development plans and serve as Clinical Pharmacology lead for programs in clinical development
• Represent the company in regulatory interactions and propose innovative strategies to accelerate therapies to patients
• Perform and/or oversee modeling and simulation to support drug development decisions
• Provide clinical pharmacology input on Phase 1–3 clinical study designs and dedicated Phase 1 clinical pharmacology studies
• Author and review clinical pharmacology sections of Investigator's Brochures, INDs, NDAs, and other regulatory submissions
• Act as clinical pharmacology expert during health authority interactions
• Interface with clinical study, translational, preclinical, and due diligence teams
• Collaborate with clinical development and discovery functions across end-to-end drug discovery and development projects

Executive Director, Clinical Pharmacology – Pharmacometrics

Vice President

• Develop and lead integrated Medical Affairs strategies for priority assets, including scientific narrative, evidence gaps, stakeholder engagement, publication strategy, medical education, advisory boards, field medical planning, and launch readiness
• Provide Medical Affairs support on cross-functional asset teams across Clinical Development, Regulatory Affairs, Development Sciences, HEOR/RWE, Biostatistics, Clinical Operations, Portfolio Strategy, Patient Advocacy, Communications, Legal/Compliance, and Business Development
• Build evidence-generation plans supporting asset differentiation, patient benefit, clinical adoption, and value demonstration
• Translate external insights from healthcare professionals, investigators, patient communities, payers, health systems, and scientific leaders into recommendations for development strategy, trial design, endpoints, education needs, and evidence priorities
• Lead scientific engagement with key opinion leaders, digital opinion leaders, investigators, cooperative groups, patient advocacy organizations, professional societies, and other external stakeholders
• Lead congress and conference strategy for priority programs, including ASCO, ESMO, AACR, AAN, and other relevant medical congresses
• Partner with data science, platform, and Decision Science teams on responsible AI-enabled approaches for medical insights, evidence synthesis, stakeholder mapping, scientific communication, and measurement of medical impact
• Establish medical communication strategies, including publications, congress abstracts and presentations, lexicon, scientific platform, FAQs, medical information content, and internal scientific training
• Design and build a structured, scalable Medical Affairs organization as the portfolio matures
• Establish governance, operating rhythms, vendor partnerships, performance metrics, and compliant processes supporting growth from clinical-stage development through launch readiness
• Report to the Chief Medical Officer and collaborate with leaders across Development, Regulatory, Development Sciences, Clinical Operations, Data Science, Biology, Chemistry, Portfolio Strategy, Communications, Legal/Compliance, and future commercialization functions

Vice President, Medical Affairs

Director

• Define and drive asset strategy for small molecule clinical programs in oncology and immunology/inflammation
• Integrate competitive positioning, mechanistic differentiation, biomarker strategy and patient segmentation into portfolio decisions
• Translate Recursion OS and ClinTech insights into strategic asset advantages
• Develop and pressure-test competitive narratives for oncology and immunology/inflammation portfolio assets
• Build evidence bases for leadership decisions, partnering discussions and investor communications
• Partner with clinical development, business development, finance and platform leaders on resource allocation
• Raise standards for advancing, differentiating and delivering assets to patients
• Operate as a senior strategic partner across Clinical Development, Discovery, ClinTech, Platform and BD
• Optimize asset positioning using AI-powered platforms, data analysis, predictive modeling, real-world evidence integration and patient stratification

Executive Director, Asset Team Lead

Supply Chain

• Lead end-to-end clinical supply chain strategy for assigned global programs
• Establish Phase I/II processes while building for Phase III pivotal-trial requirements
• Oversee clinical demand forecasting, packaging, labeling, global distribution, logistics, and inventory management
• Manage external packaging vendors, CMOs, and trial supply depots
• Implement, scale, and optimize IRT/RTSM logic for complex trial designs
• Build and improve data-driven workflows using AI and advanced tools
• Partner with Clinical Operations, Quality Assurance, Regulatory, and CMC
• Create scalable supply chain tools and SOPs
• Develop proactive risk-mitigation strategies for registrational trials and uninterrupted patient supply
• Report to the Director of Clinical Supplies as part of Recursion's Development Team

Clinical Supply Chain Manager

• Lead end-to-end clinical supply chain strategy for assigned global programs
• Establish Phase I/II processes while building for Phase III pivotal-trial requirements
• Oversee clinical demand forecasting, packaging, labeling, global distribution, logistics, and inventory management
• Manage external packaging vendors, CMOs, and trial supply depots
• Implement, scale, and optimize IRT/RTSM logic for flexible, complex trial designs
• Build and improve data-driven workflows using AI and advanced tools
• Optimize forecasting, inventory management, and logistics processes
• Partner with Clinical Operations, Quality Assurance, Regulatory, and CMC
• Align supply strategies with trial milestones and commercial readiness
• Create scalable supply chain tools and SOPs
• Develop proactive risk-mitigation strategies supporting registrational trials and uninterrupted patient supply
• Report to the Director of Clinical Supplies as part of the Recursion Development Team

Associate Director, Clinical Supply Chain

• Lead end-to-end clinical supply chain strategy for assigned global programs
• Establish Phase I/II processes and build capabilities for Phase III pivotal trials
• Oversee clinical demand forecasting, packaging, labeling, global distribution, logistics, and inventory management
• Manage external packaging vendors, CMOs, and trial supply depots
• Implement, scale, and optimize IRT/RTSM logic for complex trial designs
• Build data-driven workflows using AI and advanced tools
• Partner with Clinical Operations, Quality Assurance, Regulatory, and CMC
• Create scalable supply chain tools, SOPs, and proactive risk-mitigation strategies
• Support registrational trials, flexible protocols, and uninterrupted patient supply
• Report to the Director of Clinical Supplies

• Lead end-to-end clinical supply chain strategy for assigned global programs
• Establish Phase I/II processes while preparing for Phase III pivotal-trial requirements
• Oversee clinical demand forecasting, packaging, labeling, global distribution, logistics, and inventory management
• Manage external packaging vendors, CMOs, and trial supply depots
• Implement, scale, and optimize IRT/RTSM logic for complex trial designs
• Build and improve data-driven workflows using AI and advanced tools
• Optimize forecasting, inventory management, and logistics processes
• Partner with Clinical Operations, Quality Assurance, Regulatory, and CMC
• Create scalable supply chain tools and SOPs
• Develop proactive risk-mitigation strategies supporting registrational trials and uninterrupted patient supply
• Report to the Director of Clinical Supplies
• Help mature operational capabilities as assets progress toward commercialization

• Define and drive asset strategy for small molecule clinical programs in oncology and immunology/inflammation
• Integrate competitive positioning, mechanistic differentiation, biomarker strategy, and patient segmentation into portfolio decisions
• Translate Recursion OS and ClinTech insights into strategic asset advantages
• Develop and pressure-test competitive narratives for portfolio assets
• Build evidence bases informing leadership decisions, partnering discussions, and investor communications
• Partner with clinical development, business development, finance, and platform leaders on resource allocation
• Raise the bar on advancing, differentiating, and delivering assets to patients
• Operate as a senior strategic partner across Clinical Development, Discovery, ClinTech, Platform, and BD

Executive Director, Clinical Pharmacology/Pharmacometrics

Executive Director, Clinical Pharmacology – Pharmacometrics

Vice President, Medical Affairs

Executive Director, Asset Team Lead

Clinical Supply Chain Manager

Associate Director, Clinical Supply Chain

Associate Director, Clinical Supply Chain

Clinical Supply Chain Manager

Executive Director, Asset Strategy