Vice President, Toxicology

Company: Incyte Corporation
Location: Wilmington
Posted on: July 1, 2025

Job Description:

Incyte 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. Job Summary (Primary function) The Vice President, Toxicology oversees and manages the toxicology function within Discovery Biology in support of the organization’s goals and mission. The VP manages all activities associated with safety evaluation of small and large molecule new chemical entities, lead risk mitigation strategies, support of worldwide regulatory filings and effective communication across functions within the organization. Essential Functions of the Job (Key responsibilities) Work with toxicology project leads to define toxicology program strategies and timing for all discovery and development projects (small and large molecule), including general toxicology, developmental and reproductive toxicology, genetic toxicology, carcinogenicity and safety pharmacology. Ensure programs align with current global regulatory requirements and industry standards. Evaluation of the risk associated with toxicology/safety signals (earliest possible time) and the effective communication of the impact of the safety signal to the organization. Development and implementation of strategies to mitigate/resolve risk associated with toxicology safety signals. Active and proactive participation at the senior level of scientific, strategic, and operational aspects of drug discovery and development within the pharmacology, toxicology, and both early and late stage clinical drug development process. Oversight of the writing, review and evaluation of documents for FDA and global submissions. Manage support of regulatory filings with worldwide regulatory authorities from IND/CTA through NDA/BLA/MAA. Communication (written and oral) with regulatory agencies in response to questions arising from regulatory submissions; review and evaluation of documents for FDA and global submissions; and representing Incyte at health authority meetings. Support business development via review/due diligence of potential external assets. Support CMC as needed through safety evaluation of impurities, extractables/leachables, occupational safety evaluations (OELs, PDEs), and environmental risk assessments Manage a team of PhD toxicologists (project leads), pathologists, in-life scientists and laboratory animal staff. In-depth understanding of in vivo and in vitro biology, particularly molecular pathways in assessing risk and solving experimental questions in both pharmacology and toxicology. Qualifications (Minimal acceptable level of education, work experience, and competency) Ph.D. in Toxicology or related field. DABT certification desired. 15 years related experience at director level or above in the pharmaceutical industry or related function. Management experience Demonstrate skills in written and verbal communications; organized and detail oriented. Demonstrate a thorough understanding of ADME, CMC and clinical functions, and ability to communicate effectively across disciplines in order to facilitate understanding and rapid resolution of issues. In depth understanding of global regulatory requirements, industry standards, and emerging trends in toxicology. Experience in filing IND/CTAs and NDAs for small and large molecules. Experience in developing risk mitigation strategies for emerging safety signals and communicating impact of signals in the context of both oncology and non-oncology drug development 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. 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 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. 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, Incyte’s data protection officer, and your supervisory authority (if applicable).

Keywords: Incyte Corporation, Lower Merion , Vice President, Toxicology, Science, Research & Development , Wilmington, Pennsylvania