Medical Affairs Associate Director EMEA Skin Health H/F Kenvue

Détail du poste

Medical Affairs Associate Director EMEA Skin Health This position reports into Head, Medical and Safety Sciences, EMEA and will BE based at one of High Wycombe, UK; or Neuss Germany or Val de Reuil, France Who we are At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we're the house of iconic brands - including NEUTROGENA®, AVEENO®, LISTERINE®, JOHNSON'S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you ! Join us in shaping our future-and yours. For more information, click here. Role reports to : Head, Medical and Safety Sciences, EMEA Location : High Wycombe, UK; or Neuss, Germany or Val de Reuil, France Travel : up to 20% What you will do The Associate Director Medical Affairs Skin Health is responsible for managing the design and implementation plans of the medical affairs program for our Skin Health and related products, including budget development and tracking of all projects, managing and delegating work of the medical affairs network, and establishing accountability for assignments. You will also lead and manage the creation of educational and other materials for use by internal stakeholders, publication planning, preparation and review, and support technical learning needs of partners : Key Responsibilities · Lead and manage the Medical Affairs Network to ensure effective communication and collaboration with cross-functional teams. · Develop and implement medical strategies and plans to support the company's goals and objectives. Own the EMEA Medical Plan for assigned products · Provide medical expertise and guidance to internal and external stakeholders. · Ensure compliance with appropriate regulatory requirements and industry standards. · Contribute to the development of scientific publications, science presentations, and educational materials. · Stay up to date with the latest medical and scientific developments in the field. · Design and implement medical affairs programs to achieve organizational objectives · Provide medical and scientific leadership inputs to the innovation strategy and program of projects and, where needed, prioritize resource to the Key Countries. · Work in partnership with Health Care Professional Marketing to advance and implement effective advocacy plans with Health Care Professionals, driving recommendations and Kenvue science equity · Create educational and supporting materials for use by internal and external stakeholders · Manage and delegate work of Team members and oversee accountability for assignments · Manage assigned publications to include planning, preparation and review · Contribute technical content to Regulatory Documentation including submissions, requests for information, aggregate safety reports and product information. · Identify and build collaborative networks and partner with External HCP experts. · Represent Kenvue with external Parties including Agencies, Professional Associations, HCP Thought Leaders, Healthcare Organizations, Scientific Meetings and Consumers. · Ensure that any assigned trials/registries and other data generating activities are conducted to all applicable guidelines, regulations, company procedures with the highest ethical and quality standards · Develop and provide medical and technical information related to the company's products for use within and outside the Company · Support technical learning for partners · Manage budget planning and tracking, contract negotiation and oversight of vendor activities · Execute the company's product safety requirements including drug surveillance program which may require following up on adverse reaction reports · Maintain collaborative working relationship between medical affairs and internal stakeholders to deliver timely and expert support to product development · Lead and where needed manage a matrix group of professionals · BE a leader and advocate for our Brands · Leadership in the EMEA Medical and Safety Sciences Team, partnering with and supporting other members of the Team and wider MCSS Community · There may BE additional responsibilities supporting other Skin Health and certain Essential Health Segment products, programs and innovation projects.