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. Job Summary Primary function The Senior Manager Regulatory Submissions 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 andor 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 documentsubmission 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 Bachelors 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 writing skills are essential. Ability to manage multiple priorities and projects with support for diverse working styles and needs. Strong attention to detail and quality. Disclaimer The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties responsibilities and qualifications. Management reserves the right to change or modify such duties as required. Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer. We Respect Your Privacy Learn more at httpwww.incyte.comprivacy-policy The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate. During the process you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here. You may have the right to access delete restrict edit move or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work. You can learn more about Incytes data protection practices here. By accessing this link you can learn about the types of personal data we collect how we use it whether collection and processing is optional sources of the personal data we process how it is shared where it is stored or transferred to how long we keep it and contact information for Incyte Incytes data protection officer and your supervisory authority if applicable. Please contact privacyincyte.com if you have any questions or concerns or would like to exercise your rights.