Medical Advisor Cardiorenal - Benelux

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We are seeking a Medical Scientist to join our Cardiorenal Benelux Medical Affairs team, with a strong focus on rare disease nephrology. This role plays a critical part in shaping and executing medical strategy, ensuring a patient-centric and science-driven approach across the portfolio. The position can be based in Breda (Netherlands) or Mechelen (Belgium) and reports directly to the Head of Medical Affairs Benelux. Position Purpose: Under general direction, be responsible for the development and implementation of the Medical Affairs strategy and tactics in the designated therapy area. Provides medical expertise and input to the Business team of the designated therapeutic area to ensure targeted development of new products and optimal scientific positioning of existing products ensuring a comprehensive patient focus. Responsible for developing long-term relationships with External Experts (aka KOL) and Patients 0rganisations, and holder of KOL engagement plan. Identifies unmet medical needs and reinforces the patient focus of all medical activities. Main Responsibilities and Accountabilities: 1. Strategy Under general direction, provide input from medical affairs perspective and contribute to strategic product plans for the country. Be a part of the Business Team to develop strategic medical, scientific and relationship management plans that align with business objectives Medical input into key cross-functional groups Responsible for medical activities required for this process. 2. Interaction with Medical and Scientific Community Builds relationships and demonstrates the clinical outcome and benefits of CSL products to External Experts. Provide a high-quality single point of contact for scientific interaction between External Experts / HCP's and CSL. Respond to specific local requests for scientific and medical information in a comprehensive, timely and customer focused manner. Actively drives Scientific Advisory Board meetings to ensure knowledge transfer, foster External Expert relationships, ensure scientific understanding, and build appropriate advocac y . Actively participate in Scientific and Medical symposia. Assisting with development of CSL sponsored programs. Facilitate consideration of proposals for c ollaborative/ investigator-initiated studies. Facilitate site feasibility assessments 3. External Expert Development Under general direction, ensure development plans are initiated and actively managed for identified EE's. Facilitate speaker development and involvement locally and international l y. Ensure appropriate EE development through participation in clinical trials. Ensure communications are tracked in appropriate s y stems to ensure CSL is compliant with good governance and transparency regulations. 4. Therapy Area Expertise Develop and maintain extensive knowledge of the designated therapeutic area(s), pipeline, and the competitive landscape. Be considered an expert by internal & external customers. Disseminate knowledge and share information as appropriate (within compliance regulations), including through internal and external presentations. Provide training and education of relevant stakeholders. B e a part of the review process for materials (as required ) . Provide input into the reimbursement dossier. Provision of information to reimbursement authorities and other relevant external government/regulatory bodies as and when requested to high professional standard. 5. Ensuring actions comply with: CSL's Code of Responsible Business Practice CSL's Global Quality Policy (W000037E) Pay full attention and act along local quality system processes and procedures Local and global medical affairs processes and procedures National Industry association Deontology Code Job Qualifications and Experience Requirements: Education : University degree: Physician, Pharmacist, Master of Science in Biomedical Sciences Fluent in Dutch Prior Pharmaceutical or Biotech industry experience (medical, clinical or specialty products expertise) of at least 3 years. Abilit y t o appl y and leverage scientific and medical knowledge is essential Experience in thera p y area is desirable Strong negotiation, influencing a n d leadership skills Excellent presentation, interpersonal and communication skills Demonstrated abili t y to manage relationships with external experts Demonstrated business planning abili t y and strong organisational skills Demonstrated innovative thinking Demonstrated working knowledge of regulations governing information provision/interactions with customers within the pharmaceutical industr y . Strong medical governance capabilities. Strong strategic thinking capabilities Abilit y to work independently & be sel f- motivating The role will require some offsite attendance at meetings, conferences, exhibitions, which includes international travel. This position description provides a summary o f ke y features of the role. It may be varied as necessary

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