Senior Manager, Regulatory Operations

Overview A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. 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, Incyte has operations in North America, Europe, and Asia.

The job is based in Wilmington Delaware, US. (Minimum 3 days per week in the office. Local candidates or those willing to relocate only). Job Summary (Primary function) The Senior Manager, Regulatory Operations, is responsible for managing and maintaining existing development and marketing authorization dossiers, managing RIM objects and compiling submissions in compliance with ICH specifications and Health Authority regulations globally. The Sr Manager will coordinate with functional leads in various disciplines to ensure compliant documents, maintain regulatory information and the physical and electronic regulatory archives, mentor on eCTD requirements and other duties and/or special projects as assigned or required. Essential Functions of the Job (Key responsibilities)

Responsible for the timely planning, compiling, publishing, review and delivery of compliant regulatory submissions to Regulatory Health Authorities. Ensures documents and RIM objects comply with submission ready standards and guidelines and provides guidance with respect to requirements. Maintains and archives all regulatory correspondence in appropriate systems. Liaises with vendors for submission support, as needed. Participates in validation or verification testing of templates, electronic document management system, information management and document/submission publishing related tools. Maintains tracking tools and systems for regulatory information, including submission content plans. Support other areas of the company (eg., Business Development) concerning regulatory documentation, as needed. Maintains current working instructions for regulatory-related systems (e.g. publishing software, RIM and EDMS. Mentors team members on submission processes and requirements and may manage contract Regulatory Operations personnel. Contribute positively to a strong culture of business integrity and ethics. Act within compliance and legal requirements as well as within company guidelines. Coordinate the preparation and review of documents for regulatory submissions (e.g. cover letters, forms, DSURs, safety reports, etc.). Participates in the preparation of dossiers containing manufacturing, preclinical, and clinical data. Provides guidance to authors for clear document and data presentation and location in order to optimize submission navigation as well as the regulatory review and approval process.

Qualifications (Minimal acceptable level of education, work experience, and competency)

Bachelor's degree in a relevant field (e.g., science, technology, health, or business management) or equivalent experience. Candidates with diverse educational backgrounds are encouraged to apply. Minimum of relevant experience in a regulatory affairs environment with document management systems, electronic publishing systems, and electronic submissions, including eCTD, and direct submission to global Health Authorities. Candidates with equivalent skills and knowledge are encouraged to apply. Experience in drug development and familiarity with global regulatory submission content and formats. Experience with SPL, advertising and promotional submissions, device submissions, and combination products submissions is valued. Strong technical knowledge and proficiency in publishing and related computer software, including advanced word processing and design tools such as MS Word, Adobe, and Adobe plug-ins. Strong organizational, communication, and