OverviewWHO WE AREKintiga is a pan-European specialist that partners with ambitious health technology developers through the journey to achieve successful patient access across Europe, with a tailored approach, global perspective and local expertise. Kintiga unites three companies: MAP Patient Access (UK), AxTalis (Benelux), and SKC Consulting (Germany).What we are looking forWe are looking for a Medical Affairs & Market Access Manager in Belgium who is eager to join a growing organisation dedicated to improving patients\' lives and who has a passion for medical affairs, thrives on challenges and has excellent project-management skills. You will contribute to client projects across both domains depending on project needs. You bring scientific expertise, insights into disease and treatment trends, and the ability to engage with clinical and non‑clinical stakeholders to support patient access and pre‑/post‑launch activities. Your work may include insights generation, patient‑journey analysis, scientific and medical communication, early access activities, real‑world evidence contributions and medical education.On the Market Access side, you help secure and maintain national access for new and existing products across the Benelux region. You contribute to pricing and reimbursement dossiers, support the submission process, and collaborate on go‑to‑market strategies, advisory boards, stakeholder engagement and health‑economic materials.Key responsibilitiesManages assigned workstreams, contributes to integrating inputs into clear recommendations, and supports day‑to‑day delivery (quality, timeline, coordination).Medical Affairs activitiesContributes to go‑to‑market and medical affairs planningSupports implementation of medical tactics such as organizing CME activitiesEngage in insights collection activities (e.g., KEE engagements, Delphi panels, advisory boards)Develop medical and scientific communications such as papers, slide decks, training materials, value dossiers, etc.Maintains professional relationships with clinical and other stakeholders and supports scientific interactionsContribute to RWE activitiesEnsure compliance with legal, regulatory and company standards and codes of conduct for materials and activitiesMarket Access activitiesCo‑develop go‑to‑market and market access strategyContributes to the development of market access strategies for new price and reimbursement submissions in Benelux to gain or maintain market access (writing of reimbursement dossier, submission and support through reimbursement process)Prepares pricing and reimbursement dossiers and supports the submission processInsights generation via KEE contacts and advisory boardsProject Management and Project LeadershipContributions to cross‑functional teamsCollaborates with clients and colleagues in cross‑functional teams to support the development of patient access deliverables and related deliverables with a focus on Benelux, and willingness to contribute to projects in other geographies of the groupContributes to regulatory, medical affairs and market access projects as neededEssential requirementsMD, Pharmacist or PhD with a strong scientific background2–3 years of experience within the Belgian pharmaceutical ecosystem, ideally within medical affairs or market access, in pharma, biotech, consulting, academia or similarProven ability to build and maintain trusted and long‑term relationships with external stakeholdersSkilled at translating scientific and clinical data into clear, relevant and audience‑adapted messages for KEEs and broader audiencesConfident, respectful and solution‑oriented in navigating challenging conversations and addressing objectionsAble to work independently within defined project frameworks and manage priorities effectivelyGood project management skills and experience coordinating activities within a project teamCollaborative and inclusive mindset with proactive, analytical, strategic and client‑focused behaviourFluent in Dutch or French, and EnglishAble to exchange scientific ideas openly, constructively and with intellectual curiosity with KOLs and colleaguesExcellent presentation skills of scientific and medical data to small and large audiencesCommitted to working in full compliance with internal policies and external regulationsDesirable requirementsExperience in developing or contributing to reimbursement dossiers, HTA submissions or payer value materialsUnderstanding of real‑world evidence generation and its application in access and medical strategyFamiliarity with Belgian healthcare system dynamicsStrong digital literacy and ability to use digital tools for scientific communication and stakeholder engagementWhat we offer Competitive Salary (dependent on experience) Extensive benefit programme Company‑wide meet-ups Exposure to an international work environment with cross‑border project responsibilities Hybrid environment – 1 day per week in the office (Ghent Office on a Tuesday)⭐️ Flexible working – to help maintain a better work/life balanceWe bring together diverse backgrounds and expertise, and our team is dynamic, solutions‑focused, and committed to delivering excellence. If you are a results‑driven professional looking for an opportunity to help shape the future of a growing European business, we would love to hear from you!This role is open to full‑time applicants only.No agencies please.Unfortunately, we are unable to sponsor candidates for this role.
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