Medical Affairs & Market Access Manager

WHO WE ARE ☝🏼

We are Kintiga, a pan-European specialist that partners with ambitious health technology developers through the complex journey to achieve successful patient access across Europe, with our tailored approach, global perspective and local expertise. Kintiga unites three companies: MAP Patient Access (UK), AxTalis (Benelux), and SKC Consulting (Germany).    

WHAT WE'RE LOOKING FOR 🔍

We are looking for aMedical Affairs & Market Access Manager or Officer inBelgium who is eager to join a growing organisation, dedicated to improving patients' lives and a professional with a passion for medical affairs, who 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 (eg 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 the 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 expertise within Belgian pharmaceutical eco-system, ideally within medical affairs or market access, in Pharma, BioTech, Consultancy, 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 objection 

• 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 CAN WE OFFER YOU? 🤩

💰 Competitive Salary (dependent on experience)

🎁 Extensive benefit programme, including meal vouchers, end-of-year 13th month & mobility budget

🌴 32 days of leave (20 legal days and 12 ADV work time reduction days)

👥 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 tofull-time applicants only.
• No agencies please.
• Unfortunately, we are unable to sponsor candidates for this role.