Ph3Overview /h3pWHO WE ARE /ppKintiga 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). /ph3What we are looking for /h3pWe are looking for a bMedical Affairs Market Access Manager /b in bBelgium /b 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. /ppOn 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. /ph3Key responsibilities /h3ulliManages assigned workstreams, contributes to integrating inputs into clear recommendations, and supports day‑to‑day delivery (quality, timeline, coordination). /li /ulh3Medical Affairs activities /h3ulliContributes to go‑to‑market and medical affairs planning /liliSupports implementation of medical tactics such as organizing CME activities /liliEngage in insights collection activities (e.g., KEE engagements, Delphi panels, advisory boards) /liliDevelop medical and scientific communications such as papers, slide decks, training materials, value dossiers, etc. /liliMaintains professional relationships with clinical and other stakeholders and supports scientific interactions /liliContribute to RWE activities /liliEnsure compliance with legal, regulatory and company standards and codes of conduct for materials and activities /li /ulh3Market Access activities /h3ulliCo‑develop go‑to‑market and market access strategy /liliContributes 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) /liliPrepares pricing and reimbursement dossiers and supports the submission process /liliInsights generation via KEE contacts and advisory boards /liliProject Management and Project Leadership /li /ulh3Contributions to cross‑functional teams /h3ulliCollaborates 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 group /liliContributes to regulatory, medical affairs and market access projects as needed /li /ulh3Essential requirements /h3ulliMD, Pharmacist or PhD with a strong scientific background /lili2–3 years of experience within the Belgian pharmaceutical ecosystem, ideally within medical affairs or market access, in pharma, biotech, consulting, academia or similar /liliProven ability to build and maintain trusted and long‑term relationships with external stakeholders /liliSkilled at translating scientific and clinical data into clear, relevant and audience‑adapted messages for KEEs and broader audiences /liliConfident, respectful and solution‑oriented in navigating challenging conversations and addressing objections /liliAble to work independently within defined project frameworks and manage priorities effectively /liliGood project management skills and experience coordinating activities within a project team /liliCollaborative and inclusive mindset with proactive, analytical, strategic and client‑focused behaviour /liliFluent in Dutch or French, and English /liliAble to exchange scientific ideas openly, constructively and with intellectual curiosity with KOLs and colleagues /liliExcellent presentation skills of scientific and medical data to small and large audiences /liliCommitted to working in full compliance with internal policies and external regulations /li /ulh3Desirable requirements /h3ulliExperience in developing or contributing to reimbursement dossiers, HTA submissions or payer value materials /liliUnderstanding of real‑world evidence generation and its application in access and medical strategy /liliFamiliarity with Belgian healthcare system dynamics /liliStrong digital literacy and ability to use digital tools for scientific communication and stakeholder engagement /li /ulh3What we offer /h3ulli Competitive Salary (dependent on experience) /lili Extensive benefit programme /lili Company‑wide meet-ups /lili Exposure to an international work environment with cross‑border project responsibilities /lili Hybrid environment – 1 day per week in the office (Ghent Office on a Tuesday) /lili⭐️ Flexible working – to help maintain a better work/life balance /li /ulpWe 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! /pulliThis role is open to full‑time applicants only. /liliNo agencies please. /liliUnfortunately, we are unable to sponsor candidates for this role. /li /ul /p #J-18808-Ljbffr