Associate Director, Clinical R&D QA US

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. SUMMARY This position is responsible for providing GCP oversight of Clinical development teams to the Head of Incyte Global R&D QA. This role will also include the execution and management of Incyte QA GCP audits and the provision of GCP guidance and advice across assigned Clinical Development programs. The Senior Manager Clinical R&D QA is also the QA lead for clinical inspection activities related to the clinical programs under its quality oversight. DUTIES AND RESPONSABILITIES Provide QA GCP advice and support to Incyte Clinical Development/Operations functions and other relevant functions as assigned. Plan, schedule and conduct audits of Clinical Investigator Sites, Vendors, , Trial Master Files and Clinical submission documents. Assist with the management of QA consultants performing audits on behalf of Incyte QA. Lead regulatory authority inspections activities for development programs assigned including conducting pre-inspection audits, inspection readiness activities and coordination/hosting inspection role, as assigned. Coordinate responses and corrective/preventative actions from deviations, audit and regulatory findings. Assist with the maintenance of the clinical Quality Management System including QA support for change control, deviations, review/revision of SOPs with ensuring continuous process improvement Stay abreast of clinical trial requirements, ICH GCP, and guidelines from other regulatory agencies for the management of clinical trials as appropriate. Alert Global Clinical R&D QA Upper Management of internal and external GCP compliance and clinical trial issues in a timely manner. Mentoring Junior Clinical QA as assigned Promote Quality Culture with external R&D stakeholders, as assigned Stay abreast of local/country clinical activities/initiatives from Regional Clinical Operations members and ensure necessary QA oversight in place as Clinical R&D QA Point of contact. Conduct GCP training for Incyte staff. Be knowledgeable and be able to understand advanced operational, scientific and/or clinical research areas. Be thoroughly familiar with assigned Incyte Compounds and protocol REQUIREMENTS Bachelor’s degree in a science or healthcare related discipline, or similarly conferred degree from a university 5 to 7 years’ experience in a pharmaceutical or bio-pharmaceutical company in a GCP QA role or Clinical compliance role. Minimum of 5 years’ experience performing GCP audits of investigator sites and/or CROs English fluency written and spoken (the company language) Regulatory inspection experience as coordinator or key role Ability to travel up to 30%. Excellent written and oral communication skills. This role is office-based. 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: http://www.incyte.com/privacy-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 Incyte’s 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, Incyte’s data protection officer, and your supervisory authority (if applicable). Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.

Biopharmaceutical company discovering and developing small molecule drugs in oncology and inflammation. Headquartered in Wilmington, DE.

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