Senior Director Clinical Research Scientist

Senior Director Clinical Research ScientistIncyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rigorous pursuit of research and development excellence to improve the lives of patients, make a difference in health care, and build sustainable value.The Company strives to discover and develop first-in-class and best-in-class medicines-advancing a diverse portfolio of large and small molecules.We are seeking a Clinical Scientist to join our Early Clinical Development Group at a level commensurate with experience (Associate Director through Executive Director). This role is intentionally designed to attract both emerging leaders and experienced strategic contributors. Depending on level, you will contribute to or lead early clinical development and clinical pharmacology programs, with increasing ownership, strategic influence, and cross-functional leadership at more senior levels. You will have the opportunity to work across the full product lifecycle—from First-in-Human studies through approval and post-marketing—within a collaborative, science-driven environment that values curiosity, innovation, and continuous learning.Key Responsibilities:Core Responsibilities (All Levels)Contribute to the design, execution, and interpretation of early clinical and clinical pharmacology studiesCollaborate cross-functionally with Clinical Operations, Translational Sciences, Quantitative Clinical Pharmacology, and StatisticsSupport development of clinical documents including protocols, study reports, and regulatory submissionsAnalyze and interpret clinical safety and efficacy data in collaboration with Medical and Scientific teamsMaintain awareness of competitive landscape and emerging standards of careEnsure adherence to timelines, budgets, SOPs, and regulatory requirementsPresent data internally and contribute to external scientific communicationsAdditional Responsibilities by LevelAssociate DirectorLead components of clinical studies and contribute to program-level strategyDraft and independently own sections of key clinical and regulatory documentsCollaborate closely with cross-functional partners to execute study deliverablesPresent findings to internal teamsDirector / Senior DirectorLead clinical studies and drive cross-functional executionContribute meaningfully to clinical development strategyServe as a scientific leader on project teams and influence decision-makingMentor junior team members and contribute to team developmentExecutive DirectorProvide strategic leadership across programs or therapeutic areasShape and drive clinical development strategy and represent programs to governance bodiesInfluence portfolio-level decisions and external collaborationsServe as a recognized subject matter expert internally and externallyLead high-visibility initiatives, including regulatory interactions and scientific presentationsQualificationsMinimum RequirementsPhD, PharmD, or MD with 5+ years of relevant experience, ORBS/MS with 10+ years of relevant experienceExperience in early clinical development, clinical pharmacology, or a related disciplineStrong analytical, communication, and problem-solving skillsAbility to work independently and collaboratively in a dynamic environmentAdditional Experience by LevelAssociate DirectorExperience contributing to clinical studies and cross-functional teamsDemonstrated ability to analyze and interpret clinical dataDirector / Senior DirectorProven experience leading clinical studies or key program componentsAbility to influence cross-functional teams and contribute to strategyExecutive DirectorExtensive experience leading clinical development programsStrong track record of strategic leadership and influencing senior stakeholdersExperience representing programs in high-visibility settings (e.g., regulatory interactions, governance)Preferred Qualifications (All Levels)Experience in clinical pharmacology, immunology, or oncologyStrong scientific curiosity and a proactive, question-driven mindsetAbility to present complex data clearly and effectivelyAdditional InformationWillingness to travel up to 20% as needed (reasonable accommodations available)Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.