Overview WHO WE ARE
Kintiga 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 for We 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 responsibilities Manages assigned workstreams, contributes to integrating inputs into clear recommendations, and supports day‑to‑day delivery (quality, timeline, coordination).
Medical Affairs activities Contributes to go‑to‑market and medical affairs planning
Supports implementation of medical tactics such as organizing CME activities
Engage 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 interactions
Contribute to RWE activities
Ensure compliance with legal, regulatory and company standards and codes of conduct for materials and activities
Market Access activities Co‑develop go‑to‑market and market access strategy
Contributes 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 process
Insights generation via KEE contacts and advisory boards
Project Management and Project Leadership
Contributions to cross‑functional teams Collaborates 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
Contributes to regulatory, medical affairs and market access projects as needed
Essential requirements MD, Pharmacist or PhD with a strong scientific background
2–3 years of experience within the Belgian pharmaceutical ecosystem, ideally within medical affairs or market access, in pharma, biotech, consulting, academia or similar
Proven ability to build and maintain trusted and long‑term relationships with external stakeholders
Skilled at translating scientific and clinical data into clear, relevant and audience‑adapted messages for KEEs and broader audiences
Confident, respectful and solution‑oriented in navigating challenging conversations and addressing objections
Able to work independently within defined project frameworks and manage priorities effectively
Good project management skills and experience coordinating activities within a project team
Collaborative and inclusive mindset with proactive, analytical, strategic and client‑focused behaviour
Fluent in Dutch or French, and English
Able to exchange scientific ideas openly, constructively and with intellectual curiosity with KOLs and colleagues
Excellent presentation skills of scientific and medical data to small and large audiences
Committed to working in full compliance with internal policies and external regulations
Desirable requirements Experience in developing or contributing to reimbursement dossiers, HTA submissions or payer value materials
Understanding of real‑world evidence generation and its application in access and medical strategy
Familiarity with Belgian healthcare system dynamics
Strong digital literacy and ability to use digital tools for scientific communication and stakeholder engagement
What 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 balance
We 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.
#J-18808-Ljbffr