Medical Advisor, Dermatology

1 mese fa

Milan, Italia Incyte A tempo pieno
Overview

Words from our General Manager Italy – Onofrio Mastandrea

“Incyte is the pioneer Biotech Company in Italy for the mindset of innovation. At Incyte Italy, innovation is a set of behaviors to find new ways to overcome challenges and Solve On. Incyte is a Team where we continuously challenge the status quo and push the boundaries”.

Join our team at Incyte Italy, a dynamic and ambitious biotechnology company at the forefront of innovation in Hematology & Oncology and Immunology. We are committed to transforming lives by developing groundbreaking therapies that make a real difference.

As we continue to grow, we are seeking for a Medical Advisor to support the development of the local medical strategy and medical plans within the therapeutic area of dermatology.

Duties and Responsibilities

Builds expertise in the assigned IAI areas (derma entities, drugs) and creates/ summarizes medical insights for Italy in these areas regarding available literature, treatment options, disease environment and product data. Manages and lead the implementation of the medical/non-promotional plans for respective products. Reviews and critically appraises scientific literature and provides support and advice to medical and marketing groups in developing strategy and tactical implementation of planned activities. Provides medical and scientific input to projects and manages related activities (e.g. educational projects, communication campaigns, scientific symposia etc.). Ensures that Health Care Professionals (HCPs) and educational activities are of high scientific quality and are in line with compliance regulations. Manages external collaboration and engagement plan and country Key External Experts (KEEs) advocacy through provision of medical information. Designs and implements clinical research projects within defined standards and budgets (e.g. Phase IV, post marketing clinical activities such as registry/database projects, epidemiological surveys and PMOS studies). Provide the required oversight to manage review, approval and conduct of IIR studies. Supports the affiliate Clinical Research Department in the management of clinical studies, as appropriate (e.g. review new clinical study protocols, identifying potential investigators/sites, conducting feasibility surveys). Supports adaptation of EU/local training and scientific material in collaboration with marketing and other internal stakeholders. Supports development of publication plans and covers country data generation needs. Provides scientific in-house training for MSLs, Key Account Managers, Clinical Development and other staff. Gives medical input into local brand planning processes and is part of respective brand teams. Screens relevant literature and other information from relevant scientific societies meetings and conferences and develop summaries of key messages for use within the Company (e.g. key areas of scientific/company interest, new trends in diagnosis, monitoring and treatments in the therapeutic area, etc.). Manages planning, preparation and execution of advisory boards. Works in a cross-functional team on a national and European level. Contributes positively to a strong culture of business integrity and ethics and embraces the Mission, Vision and Values of the organization. Acts within compliance, regulatory and legal requirements as well as within company guidelines.

Requirements

Relevant scientific degree (medicine, life sciences or equivalent), MD or PhD preferred Prior experience in a Medical Affairs or similar position in the pharmaceutical industry Minimum 4 years of relevant working experience in similar roles. Experience in Dermatology / Immunology (preferred) and understanding of customer- and market needs. Knowledge in development and implementation of clinical trials. Experience of working in a cross-functional team. Excellent written and spoken communication and presentation skills . Structured approach to project management. Ability to work independently and effectively in complex, rapidly changing environments. Analytical mind setting, entrepreneurial approach, hands-on. Office based role, with ability to travel up to 25% of working time. Excellent spoken and written English. Proficient in Microsoft Office.

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.

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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 .

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 . 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@ if you have any questions or concerns or would like to exercise your rights.

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