Director / Associate Director Companion Diagnostics Lead, Translational Sciences

Overview A global biopharmaceutical company on a mission to solve unmet medical needs, Incyte follows science to find solutions for patients. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first‑in‑class medicines for patients and a strong pipeline of products in Hematology, Oncology, and Inflammation and Autoimmunity. Headquartered in Wilmington, Delaware, the company operates across North America, Europe, and Asia. Job Summary (Primary function) Associate Director, Companion Diagnostics Lead is a leadership role responsible for developing and implementing clinical diagnostic plans, including companion diagnostics (CDx) requirements within drug development programs. The role involves active participation in CDx strategy setup and deployment, managing logistics, vendor selection and relationships, and ensuring timely CDx delivery. Key Duties Serve as subject matter expert in the CDx development process (from concept to commercialization) Lead the selection and management of diagnostic partners Monitor assay analytical and clinical performance evaluation activities Author CDx‑related parts across documents Ensure CDx representation in cross‑functional teams Act as alliance and project manager between Incyte and key diagnostic partners Generate and review new project agreements as needed Manage and maintain the CDx budget for projects Track and approve milestones for each project Lead Joint Project Team (JPT) meetings with alliance partners Supervise the validation and implementation of clinical trial assay (CTA) at the testing laboratory Maintain alignment between the diagnostics partner and testing laboratory Ensure timelines are met Oversee operational aspects of clinical implementation Ensure compliance with regulatory and ethical guidelines Develop and apply expertise in regulatory requirements for CDx across regions (US FDA, EU IVDR, etc.) Supervise Incyte review of CDx documentation such as clinical study performance plans (CSPP), Instructions for Use, etc. Ensure creation and review of informed consent, CPSP, and country submissions/responses are timely and compliant Develop and maintain expertise in the delivery of Companion Diagnostics Maintain relationships with key stakeholders Qualifications Minimum qualifications: BS Degree in a scientific discipline with 7+ years of experience in the diagnostic and/or pharmaceutical industry (clinical studies). Understanding of Good Clinical Practices (GCP) and relevant regulatory requirements; ability to manage external research activities through CROs and collaborators. Ability to balance execution of multiple tasks to accomplish program goals. A high level of emotional intelligence and willingness to work closely and collaboratively with other functional groups internal and external to the company. Exceptional verbal and written communication skills. Preferred Qualifications Advanced degree in a scientific discipline with extensive experience in CDx development, registration, and commercialization and IVD clinical studies. Extensive knowledge of assay development using next‑generation sequencing, PCR, and immunohistochemistry. Experience in CDx and/or precision medicine, including IVDR. Incyte Corporation is committed to creating a diverse environment and is proud to be an equal‑opportunity employer. #J-18808-Ljbffr Incyte Corporation