Job Description
Overview 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 Manager, Medical Information and Content Development is responsible for the identifying needs and development of US Medical Affairs scientific exchange materials for field-based US Medical Affairs staff (i.e., Medical Science Liaisons, Health Outcomes Liaisons), ad hoc medical meetings, advisory board materials, content for internal staff training, medical congresses and other relevant projects and programs consistent with the Medical Affairs Strategic and Operational Plan. In addition, the role will support Medical Affairs social media activities. The Manager/Sr Manager will also provide operational oversight for the non-promotional material review process and assist with content management system administration. The position will report directly to the Executive Director, Medical Information and Content Development. Essential Functions of the Job (Key responsibilities) · Collaborates with cross-functional partners (eg, Research & Development, US/Global Medical Affairs, Publications & Medical Communications), and assists with development of scientific exchange materials for emerging therapeutic areas. · Assists with development of Medical Affairs social media content in collaboration with Medical Affairs, Publications, Global Communications, and third-party agency partners. · Assists with planning and execution for US Medical Affairs-led advisory boards. · Works cross-functionally to develop enduring scientific content related to research targets, investigational agents, and clinical study recruitment. · Serves as non-promotional review meeting coordinator, including setting agendas, establishing and deploying project workflows, capturing reviewer comments, and rendering project verdicts · Serves as content management system administrator, providing access to users, providing general system oversight, and maintaining best practices documents · Develops and maintains expertise in relevant hematology and oncology therapeutic areas, including disease states, treatment landscape, and ongoing research strategies. · Provides medical literature surveillance and oversight for US Medical Affairs and identifies and communicates pertinent updates in a timely manner. · Manages external vendors, including those involved in scientific content development and advisory board execution, and participates in the review and selection process. · Participates in the creation and maintenance of departmental SOPs and other guidance documents necessary to ensure highest levels of quality, compliance, and operational efficiency. · Assists with creation of medical information standard response letters, product dossiers, and frequently asked question (FAQ) documents, as needed. Qualifications (Minimal acceptable level of education, work experience, and competency) · Advanced scientific or clinical degree in the life sciences (eg, PharmD, PhD); the ideal candidate has 2 years' experience working in a Medical Information/Medical Affairs capacity for a pharmaceutical, medical device, medical communications company, or equivalent experience. · Experience creating scientific content, including disease state and product-related slide presentations, is required. · Knowledge of FDA regulations regarding the dissemination of Medical Information and drug promotion, is required. · Excellent oral and written communication skills are required. · Excellent project management skills, including the ability to plan, prioritize, and execute multiple projects are required. · Experience in hematology/oncology is strongly preferred. · Approximately 15% travel commitments. 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.