Descripción Key Responsibilities:Lead the development and implementation of the overall medical strategy for the vaccine portfolio, ensuring alignment with corporate goals and market needs.Continuously assess and adapt the medical strategy to respond to changes in the market, regulatory environment, and scientific advancements.Establish and maintain strategic relationships with territorial entities, government bodies, and the Ministry of Health to ensure the inclusion and promotion of the vaccine portfolio in public policies and health programs.Participate in meetings and working groups with health authorities to influence decisions related to immunization and public health policies.Develop and maintain strong relationships with Key Opinion Leaders (KOLs), medical associations, and relevant organizations to foster acceptance and appropriate use of vaccines.Organize and participate in educational events, symposiums, and conferences to position the company's vaccines as preferred options within the medical community.Collaborate with the marketing team to design and implement strategies that promote the vaccine portfolio, aligning medical objectives with market needs.Ensure that marketing strategies are backed by solid scientific evidence and comply with local and international regulations.Oversee and coordinate pharmacovigilance activities, ensuring continuous monitoring of vaccine safety and effective management of adverse event reports.Ensure compliance with all regulatory obligations related to pharmacovigilance and maintain open communication with health authorities.Lead the planning, execution, and monitoring of strategic projects related to the vaccine portfolio, ensuring alignment with corporate and medical objectives.Coordinate multidisciplinary teams, facilitating communication and collaboration across departments to ensure project success.Continuously track project progress, regularly reporting to senior management and proposing strategic adjustments as necessary.Work closely with the regulatory team to facilitate the registration of biological products with the relevant authorities.Ensure that all documents and processes necessary for regulatory approval are accurate and complete.Maintain constant and effective communication with Invima, ensuring that submissions and registration requests meet local requirements.Support the design and implementation of access strategies that enable the inclusion of vaccines in public health plans and essential medicine lists.Perfil buscado (h/m)The successful candidate should have bachelor's degree in medicine and at least 5 years of experience in similar roles within the pharmaceutical or biotechnology industry, with a focus on vaccines and project management.
A dynamic and results-oriented professional with experience in managing strategic projects and a deep understanding of the regulatory and public health environment in Colombia.Qué OfrecemosBecome part of an important worldwide pharmaceutical company.
