descriptif du posteEn tant que Technicien AGA (Appareils et Gaz Médicaux / Assistance Respiratoire), vous êtes le maillon essentiel entre les équipements de pointe et les patients à leur domicile.Au quotidien, vos activités principales :Livraison & Installation : Installer le matériel médical au domicile des patients en respectant les normes de sécurité.Formation & Conseil : Former le patient et son entourage à l'utilisation du matériel et aux consignes de

À propos de B. Braun B. Braun propose des dispositifs médicaux et des solutions de soins couvrant de nombreuses aires thérapeutiques. Présent dans plus de 60 pays, le groupe conçoit, fabrique et distribue des produits de santé destinés à améliorer la sécurité des soins et la qualité de vie des patients. Vocation Le Technicien SAV est un professionnel chargé, en Atelier, de l'installation, de la maintenance et de la réparation des dispositifs médicaux (instruments chirurgicaux, moteur de bloc opératoire, appareils de perfusion, colonne vidéo, microscope chirurgie AEOS) utilisés dans les Hôpitaux, Cliniques, Laboratoires ou cabinets médicaux. Vous serez principalement affecté sur la Gamme AIS (pompes et pousse-seringues, ...) Activités principales - Réaliser la maintenance préventive - Vérifier la conformité et la sécurité des appareils - Mettre à jour les logiciels - Diagnostiquer les pannes - Réparer ou remplacer les pièces défectueuses - Tester les appareils après intervention - Respect des normes - Rédiger des rapports d'intervention - Gérer le suivi des équipements

Centre ophtalmologique et médical situés à Toulouse, recherche un(e) secrétaire motivé(e) et autonome, pour intégrer une équipe jeune et dynamique pour un contrat CDI à temps complet de 39h/semaine. Jours de travail du lundi au vendredi. Vous savez accueillir et renseigner les patients, planifier les activités (agenda des consultations, convocations, etc.) Gérer, saisir et classer les informations relatives au dossier patient et de l'activité du cabinet. Vous savez également réaliser la facturation avec les cartes vitales. Responsabilités : - accueillir les patients, veiller à leur réception par les médecins ; - répondre aux appels téléphoniques, les transmettre si nécessaire ; - prendre les rendez-vous, gérer le planning avec les praticiens ; - saisir les comptes rendus médicaux, les courriers . ; - créer et gérer les dossiers médicaux des patients ; - assister les médecins et paramédicaux dans les actes de gestion courante (gestion des stocks et commandes de petites fournitures, gestion des factures, ...). Exigences : - Expérience préalable en tant que secrétaire médical(e) est préférable - Excellentes compétences en communication écrite et orale - Capacité à travailler de manière autonome et à gérer plusieurs tâches simultanément - Connaissance des logiciels de gestion médicale est un plus - Sens de l'organisation et souci du détail Très bonnes conditions de travail, espace moderne. Une expérience réussie au sein d'un cabinet ou centre ophtalmologique serait appréciée. Déplacement occasionnel vers un autre centre médical. Avantages : - Participation au Transport - Titre-restaurant - Mutuelle Si vous êtes une personne motivée, organisée et passionnée par le domaine médical, nous serions ravis de vous rencontrer. Type d'emploi : Temps plein, CDI Rémunération : 2100€ par mois

The AO is a medically guided, not-for-profit organization, a global network of surgeons, and the world's leading education, innovation, and research organization specializing in the surgical treatment of trauma and musculoskeletal disorders. We are home to people from all over the world, from different backgrounds, with diverse talents and specialist areas. What binds us together is our passion for excellence, our dedication to our mission of improving patient care, and our understanding that we are stronger together: we are one AO. For more information, visit: https://www.aofoundation.org/ The AO Innovation Translation Center (AO ITC) streamlines and drives innovation projects. Its activities include the development of clinical solutions with our industrial partner, innovation gathering, proof-of-concept studies, strategic investment in intellectual property, technology, or companies, and evidence creation through clinical research. As part of the AO ITC, Clinical Operations is the AO’s service provider for clinical research. Our clinical research specialists deliver clinical insights that are highly relevant to current surgical practice and enable better patient care by planning and conducting global clinical trials. The Head of Medical Scientific Affairs provides strategic and scientific leadership for AO's clinical evidence generation ecosystem and ensures that clinical research investments translate into meaningful improvements in patient care. He/she serves as a trusted scientific advisor to AO leadership, governance committees, and clinical divisions and represents AO ITC in internal and external scientific initiatives, partnerships, and expert forums. The role is accountable for developing a high-impact portfolio of clinical studies across Trauma, CMF, Spine,TC, Veterinary, and related orthopedic disciplines, ensuring optimal allocation of resources, scientific excellence, and supporting effective translation of evidence into clinical practice. The position serves as a key interface between surgeons, researchers, clinical operations, governance bodies, industry partners, and educational stakeholders to maximize the generation, dissemination, and adoption of evidence-based innovations within the AO ecosystem. Main Responsibilities: Lead the Medical Scientific Affairs team Provide scientific, strategic and operational leadership to the Medical Scientific Affairs team with two direct reports, fostering a high-performing, collaborative, and service-oriented culture. Define team objectives, priorities, and performance expectations aligned with the organization's strategy and portfolio needs. Recruit, develop, coach, and evaluate team members to support professional growth, ensuring the appropriate scientific, clinical, and operational competencies are in place. Close collaboration with Clinical Operations in the resource planning and allocation across studies, programs, and stakeholder requests to meet organizational objectives. Build effective collaboration between surgeons, governance bodies, Clinical Operations, NCR, AO Education Institute, AO Research Institute, educators, and external partners to advance the Clinical Research activities in the AO. Drive continuous improvement of Medical Scientific Affairs processes, standards, and capabilities to enhance quality, efficiency, and impact and establish a culture of scientific excellence, integrity, compliance, and evidence-based decision-making across all Medical Scientific Affairs activities. Lead the Clinical Science Advisory Commission (CSAC). Lead the AO ITC Clinical Research Fellowship Program. Support the AO PEER program. Clinical Study Design & Scientific Support Develop clinical study protocols addressing important knowledge gaps and clinical needs in close collaboration with surgeons, industry partners, governance bodies and Network Clinical Research and Clinical Operations. Review and provide medical-scientific assessment of adverse events and safety-related findings throughout study conduct. Provide expert advice on medical and scientific questions arising during study execution and support preparation of scientific publications, clinical reports, congress abstracts, and other dissemination activities. Close collaborate with Clinical Operations in study planning, implementation, and monitoring activities. Support interpretation of results in close collaboration with surgeons, investigators, governance bodies, and Clinical Operations. Drive excellence in scientific publication strategies, congress presentations, and dissemination activities. Clinical Research Portfolio Strategy Lead scientific discussions regarding future evidence needs. Develop and maintain a strategic clinical research portfolio in collaboration with the Research Commissions and internal stakeholders which is aligned with AO's mission and priorities. Establish and continuously refine portfolio prioritization frameworks balancing available research funding, knowledge gaps, patient impact, scientific significance, feasibility, cost-effectiveness and translational potential and risk-benefit considerations in collaboration with the Research Commissions and internal stakeholders. Monitor portfolio performance with regards to strategic objectives and adapt research priorities based on emerging evidence, and clinical needs. Provide scientific leadership across the full research lifecycle, ensuring methodological rigor, clinical relevance, regulatory compliance, and ethical conduct. Collaborate with Clinical Operations in establishing a grant acquisition strategy and strengthen industry partnerships and drive grant acquisition. Support Knowledge Translation activities to ensure clinical evidence generated by AO is effectively translated into education, clinical guidelines, decision support tools, and clinical practice. Collaborate closely with Clinical Operations, NCR, AO Education, AO Clinical Divisions, community development and governance bodies to facilitate adoption of new evidence. Lead implementation of health economic and outcomes research initiatives. Main Requirements: Professional & Technical Skills Advanced expertise in clinical research methodology. Strong understanding of orthopedic clinical practice and research. Advanced expertise in clinical study design, statistical principles, and evidence synthesis. Experience in designing and executing industry sponsored clinical studies as a CRO. Experience in health economic evaluation and outcomes research. Excellent scientific grant and publication writing and presentation skills. Sound understanding of regulatory requirements, Good Clinical Practice (GCP), and clinical research governance. Education & Qualifications Medical Degree (MD) required. PhD, MSc, or equivalent advanced scientific qualification highly desirable. Formal training in clinical epidemiology, research methodology, biostatistics, or related disciplines is advantageous. Professional Experience Minimum 10 years of experience in clinical research within orthopedics, trauma, spine, CMF, sports medicine, or related disciplines. Experience in multicenter clinical studies from concept generation to publication and dissemination. Experience in developing and managing research portfolios and clinical research strategies. Strong track record of peer-reviewed scientific publications and grant acquisition. Experience in line management and leading interdisciplinary and cross-functional teams. Demonstrated ability to collaborate effectively with surgeons and international clinical research networks. CRO services are of advantage. We offer: An interesting and varied job in an exciting and innovative organization The opportunity to be part of a highly committed international team Modern infrastructure High degree of flexibility regarding working hours and location (depending on operational requirements) Generous package of social benefits, including supplementary vacation days and pension scheme contributions Internal skills training opportunities and support for continued education

About the role: - Provide strategic program leadership for the most critical and complex Medical priorities, ensuring that enterprise Medical strategies are translated into executable portfolio plans, governed effectively, and delivered with visibility, accountability, and disciplined decision-making. - Serve as a senior PMO partner to Therapeutic Area and Medical leaders, shaping execution models, governance architecture, and cross-functional alignment for major programs, portfolios, launches, transformations, and lifecycle priorities. - Improve enterprise execution confidence by integrating milestone management, dependency control, risk signaling, budget visibility, and escalation leadership across highly matrixed Medical environments. - Strengthen the Medical PMO operating model by defining standards, mentoring talent, and advancing data-enabled, GCM-forward execution practices that improve speed, transparency, and consistency at scale. How you will contribute: - Lead end-to-end execution management for the most strategically important Medical portfolios or programs, establishing integrated roadmaps, governance structures, milestone frameworks, and escalation pathways that support enterprise delivery confidence. - Partner with senior Medical leaders to shape execution strategy for complex initiatives, ensuring that portfolio priorities are converted into realistic, sequenced plans with clear accountabilities, resource assumptions, interdependency management, and decision forums. - Provide enterprise-level visibility into execution health for assigned scope, synthesizing milestones, budget implications, risks, dependencies, and organizational constraints into clear leadership narratives and recommended actions. - Drive portfolio-level governance and decision-making by facilitating high-value leadership discussions, surfacing trade-offs, aligning stakeholders around choices, and ensuring timely closure of critical decisions. - Own the most complex risk and issue management topics within assigned scope, including systemic barriers, cross-program conflicts, resourcing tensions, and execution risks that require senior intervention or enterprise coordination. - Guide prioritization and scenario planning with Medical leaders and PMO leadership, helping determine where to accelerate, sequence differently, de-scope, or escalate in order to protect enterprise objectives and delivery credibility. - Provide strategic oversight of budget and resource implications for assigned portfolios, partnering with Finance and business leaders to assess execution feasibility, spending pressures, and trade-offs linked to critical path delivery. - Shape and improve the Medical PMO operating model through refinement of standards, decision-rights, governance cadences, reporting frameworks, and digital or automation-enabled execution practices. - Model Takeda values and reinforce a culture of integrity, scientific credibility, inclusion, accountability, and continuous improvement in all PMO activities. Skills and qualifications: - Bachelor's degree required; advanced degree in science, business, operations, engineering, or management preferred. - 12-14+ years of relevant experience in pharmaceutical, biotech, healthcare, or other regulated environments, including extensive leadership of complex global programs or portfolios. - Proven experience partnering with senior leaders to shape execution strategy and guide major portfolio decisions in matrixed organizations. - PMP, PgMP, change management certification, or comparable advanced PM/portfolio credentials preferred. - Strategic execution leadership: translates enterprise priorities into delivery models, governance, and portfolio control mechanisms. - Enterprise portfolio insight: identifies patterns, trade-offs, and systemic execution risks across multiple programs. - Executive communication: frames status, implications, options, and recommendations in a concise, leadership-ready manner. - Organizational influence: aligns senior stakeholders and drives action through credibility, judgment, and structured facilitation. - PMO leadership and talent development: strengthens standards, coaches others, and advances a data-enabled, future-ready execution model. - Digital enablement mindset for PMO: Embeds a digital enablement mindset across the PMO, leading adoption of digital tools, automation, and data-driven practices to transform operations, improve decision-making, and drive scalable execution.

Medical Director \- Diabetes/AID Systems (m/f/d) Medical Director – A Unique Leadership Role for Physicians in MedTech Introduction Our client, headquartered in central Switzerland is a global MedTech company focused on integrated solutions for people with diabetes. The growing organization offers a challenging and dynamic environment characterized by a clear strategic direction, ambitious growth objectives, and a high degree of personal accountability. These factors create exciting opportunities for the successful candidate in the newly created position Medical Director – Diabetes/AID Systems (m/f/d) Your responsibilities The Medical Affairs department connects clinical science, medical expertise, and real\-world application to support the successful development, differentiation, and adoption of innovative diabetes technologies. Through clinical evidence, scientific engagement, medical strategy, training and education, as well as collaboration with internal and external stakeholders, the department enables safe, effective, and patient\-centric solutions worldwide. At the core of your role is ensuring the safe, effective, and consistent clinical application of our client’s innovative AID system across global markets. You will own the development and continuous evolution of the global Training \& Education strategy, ensuring that healthcare professionals, affiliates, and internal stakeholders are equipped to support the optimal use of the company’s technologies. Through close collaboration with the key departments, including Product Management, Research \& Development, Regulatory Affairs, Commercial, and external experts, you will translate clinical expertise into best practise, support product differentiation, and contribute to the successful adoption of our client’s solutions globally. Beyond educational leadership, you will also serve as a trusted medical authority and sparring partner to key departments. Your medical insights will help shape product innovation and development, clinical differentiation, and long\-term medical strategy. As an ambassador for the organization, you will represent the company at national and international congresses, scientific meetings, advisory boards, and further professional forums. In your role as a medical/scientific spokesperson you will build and maintain strong relationships with healthcare professionals, KOLs, scientific societies, and other external stakeholders, further strengthening the company’s scientific reputation and market position. As the leader of the Global Training \& Education and Clinical Application team, you will play a pivotal role at the intersection of clinical science, product development, and commercial execution. Reporting directly to the Head of Global Medical Affairs, you will be based at the company's Swiss headquarters, with a flexible hybrid working model. The role requires approximately 20% international travel. Your identity We are seeking a dynamic and entrepreneurial physician with substantial experience in diabetes technology, including AID systems, CGM, and digital diabetes solutions. You hold a medical degree and a certification in Endocrinology/Diabetology and have developed a strong track record either in clinical settings or within the MedTech industry. Your strategic mindset, analytical approach, and ability to communicate complex medical concepts make you an effective partner for both, internal and external stakeholders. You are confident in working across functions, creating alignment between stakeholders, and influencing decisions in collaboration with the key departments, and senior leadership. Your prospects The fascinating environment of a globally expanding industry leader offering challenging opportunities and a high degree of self\-responsibility in an environment of highly motivated top\-class professionals awaits you, allowing you to significantly contribute to the company’s further growth and success as a global player. In addition to a highly visible international leadership role, there may be flexibility to maintain selected clinical responsibilities on a part\-time basis. If you can identify yourself with the requirements of this challenging position, we kindly ask you to send us your application and CV indicating the reference 3120618\. For further information please contact Dr. . Contact oprandi \& partner ag, personnel recruitment, KONNEX Building Brown Boveri Strasse 7, CH\-5400 Baden Phone \+41 79 408 68 64, [Write an email](<>), oprandi \& partner is an international group with numerous branches in Europe and the UAE / Dubai Apply jpidb681712jm jit0728jm jiy26jm

Director, Integrated Product Medical Lead (m/f/d) At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where ,Health for all, Hunger for none' is nolonger a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives ofthose around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you'rehungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice. Director, Integrated Product Medical Lead (m/f/d) YOUR TASKS AND RESPONSIBILITIES The Integrated Product Medical Lead (IPML) is crucial for advancing the Oncology early development portfolio. As an IPML, you create a significant impact through the successful progression of global development programs and the expansion of our pipeline. You set the vision and strategic direction for assigned programs, ensuring a medically and clinically sound end\-to\-end development strategy for our products across various modalities, biologies, and indications, representing the full value chain from pre\-D1 up to hand\-over to late\-stage drug development. You build an end\-to\-end clinical strategy and are responsible for executing development programs on behalf of Early Clinical Development Oncology (ECDO), providing clinical\-scientific leadership for one or more global development programs with full decision\-making authority. Collaborating with cross\-functional IPT members, you drive the creation and maintenance of a target product and target value profile to maximize the clinical success of development programs, significantly shaping the value of the product. You co\-lead the incorporation of novel assets into the pipeline through supporting internal and external innovation efforts. Additionally, you play a vital role in shaping functional excellence within ECDO by driving core project, people, and innovative clinical development topics under a peer\-reviewed setting, pushing the boundaries of drug development in collaboration with internal and external researchers. Key tasks: Act as the clinical leader and primary clinical representative for global programs, ensuring high quality and speed of functional deliverables. Develop a clinical vision for addressing unmet medical needs, considering the molecule's scientific hypothesis. Accountable for timely delivery of milestones, mitigating roadblocks, and empowered to take decisions to effectively execute the clinical strategy. Support preclinical evaluation and validation of new oncology assets in line with the Research and Early Development Oncology (RED ONC) strategy. Guide preclinical asset development to enable informed clinical development, facilitating go/no\-go decision making. Review key study documents, ensuring alignment with clinical development plans and target product profiles. Provide comprehensive knowledge of the scientific, development, and regulatory landscape to enable state\-of\-the\-art early precision drug development. Proactively interact with academic and industry partners, health authorities, key opinion leaders, and patient advocacy groups. Lead and drive ECDO\-initiated strategic initiatives in support of overall ECDO, RED\-ONC, Oncology, and Bayer strategy. Independently lead self\-empowered matrix teams, promoting a creative and innovation\-friendly collaboration between clinicians and scientists. Foster a culture of ownership and empower others, driving peer accountability across portfolio deliverables. WHO YOU ARE Medical excellence: M.D. with 5\+ years in direct patient care and board certification within oncology/hematology or associated subspecialties. Scientific excellence demonstrated by a track record of relevant research documented in peer\-reviewed publications. Outstanding drug development expertise with 3\-5 years of experience, including 2\+ years in early drug development. Expertise across different biologies and modalities, including small and large molecules. Relevant global health authority interactions and current knowledge of regulatory review and responses. Ability to independently develop a sound medical strategy and teach others to do so. Strong communication and leadership skills, strategic thinking, and good business and external trends insights. High energy with focus and vision; self\-motivated with a high sense of ownership and proactive, solution\-oriented approach. Fluency in English is mandatory; command of a second major European language, especially German, would be an asset. jpid94d3b8fjm jit0728jm jiy26jm

RaySearch develops innovative software solutions to improve cancer care. About 1000 clinics in more than 40 countries use RaySearch software to improve treatments and quality of life for patients. RaySearch was founded in 2000 and is listed on Nasdaq Stockholm. The headquarters is located in Stockholm, with subsidiaries in the US, Europe and Asia - Pacific. Today we are more than 400 employees with a common vision of improving cancer care with innovative software. Our great staff is crucial for our success and we offer a fantastic working environment in modern offices, flexibility and good opportunities for development. We believe in equal opportunities, value diversity and work actively to prevent discrimination. Are you a driven regulatory professional who enjoys ownership, collaboration and working close to product development? This could be the role for you. Apply and help shape the future of medical device software at RaySearch. About the role We are looking for an experienced and driven Regulatory Lead to own the regulatory strategy and lifecycle oversight for one of RaySearch's products. In this role, you will be the regulatory point of contact for the product, working closely with key stakeholders in the Development, Corporate Strategy and Sales teams. You will help shape product strategy, guide development activities, drive market access, and ensure compliance throughout the product lifecycle. This is a highly visible role for someone who enjoys combining deep regulatory expertise with strategic thinking, project coordination, and collaboration across the organization. What you'll do Own and drive the global regulatory strategy for your product throughout its lifecycle. Lead the preparation, review, and maintenance of Technical Documentation and regulatory submissions, including EU MDR. Act as the regulatory expert within development projects and ensure regulatory requirements are integrated throughout the design and development process. Coordinate and oversee multiple projects, priorities, and submission timelines while maintaining a long-term view of the product roadmap. Partner closely with Development, Corporate Strategy, Sales and other key stakeholders to support product development and market access. Support inspections, audits, post-market activities, and continuous improvements. Your profile You are a proactive and pragmatic regulatory professional who enjoys taking ownership and driving things forward. You are technically strong, comfortable working with development teams, and able to translate complex regulatory requirements into practical solutions. You like having oversight of the full product picture—from early development and regulatory strategy to submission and post-market activities—and you thrive in a collaborative, fast-paced environment where you can make a real impact. Requirements Bachelor's or Master's degree in Engineering, Life Sciences, Biomedical Engineering, Regulatory Affairs, or a related field. Several years of Regulatory Affairs experience within the medical device industry. Strong experience preparing and reviewing Technical Documentation under EU MDR. Experience working with medical device product development and design control processes. Experience with medical device software Strong knowledge of IEC 62304, IEC 60601 and ISO 14971 Strong project management and stakeholder management skills. Ability to manage multiple activities and timelines while maintaining the bigger picture. Proficiency in English. Meriting experience US regulatory experience, Experience with FDA submissions, including eSTAR/510(k). Experience with IEC 62366 and ISO 14155 Experience with Cybersecurity requirements for medical devices. Experience with AI/ML-enabled medical devices. Our Culture Culture at RaySearch is the driving force behind our organization, where everything we do is driven by a shared passion for innovation and the fight against cancer. Our dedication is reflected in our ability to deliver exceptional results, pay close attention to detail, and consistently go the extra mile. Our employees stand out as experts in their field, driven by a relentless focus on solving problems - no matter how complex. At RaySearch, we take pride in leading the way in cancer treatment, leveraging cutting-edge technology to develop innovative solutions that make a real difference in patient care. Our Offer At RaySearch, we offer a diverse and inclusive work environment, fostering openness, sincerity, and collaboration. Located in Hagastaden, Stockholm's Life Science Hub, our modern and creative workspace includes an in-house gym, yoga, and social activities like ping pong, table football, and regular after-work events. Our bistro serves a fantastic lunch buffet, and we offer morning- and afternoon-fika every day. Our rooftop terrace also provides a stunning 360-degree view of Stockholm, enhancing the work experience. All of this comes attached with a competitive compensation and benefits package. Application Please apply to the position through the application form below. Selection and interviews will be ongoing. We do not accept applications by e-mail.

RaySearch develops innovative software solutions to improve cancer care. About 1000 clinics in more than 40 countries use RaySearch software to improve treatments and quality of life for patients. RaySearch was founded in 2000 and is listed on Nasdaq Stockholm. The headquarters is located in Stockholm, with subsidiaries in the US, Europe and Asia - Pacific. Today we are more than 400 employees with a common vision of improving cancer care with innovative software. Our great staff is crucial for our success and we offer a fantastic working environment in modern offices, flexibility and good opportunities for development. We believe in equal opportunities, value diversity and work actively to prevent discrimination. We are looking for a Business Development Manager – Medical Oncology to help define and drive RaySearch's expansion into the Medical Oncology market. This is a unique opportunity to join RaySearch at an early stage of a new strategic growth initiative. As we explore opportunities beyond our traditional radiation oncology business, you will play a key role in helping shape our strategy, evaluate market opportunities, define commercialization approaches, and support the successful introduction of future solutions into the Medical Oncology landscape. About the job You will translate strategic direction into concrete market activities, ensuring strong alignment between product positioning, customer needs, and commercial execution. Your main tasks Lead market intelligence activities to develop a comprehensive understanding of the Medical Oncology landscape, including market dynamics, customer needs, competitive positioning, treatment pathways, reimbursement models, and emerging trends Identify and evaluate growth opportunities, unmet needs, and strategic market segments within Medical Oncology Develop and execute market development and commercialization strategies for future Medical Oncology solutions Build and maintain relationships with key stakeholders including Medical Oncologists, Oncology Nurses, Hospital Administrators, Cancer Centers, Professional Societies, and Industry Partners Assess emerging clinical evidence, technology trends, and evolving standards of care to identify opportunities for innovation and growth in alignment with the overall RaySearch ecosystem. Support customer discovery activities to ensure future solutions address meaningful clinical and operational challenges Conduct market assessments, competitive analysis, and business case development to support strategic decision-making Support the development and execution of go-to-market strategies for future product launches Identify and assess strategic partnership opportunities that support growth objectives Monitor competitive developments, market access considerations, and industry trends relevant to Medical Oncology Your Profile You are commercially minded, strategically driven, and passionate about improving cancer care. You bring a strong understanding of the Medical Oncology environment and are motivated by the opportunity to help shape a completely new business area for RaySearch. You enjoy working in situations where there is ambiguity, and you are comfortable helping define strategy, build relationships, and create new opportunities from the ground up. You are equally comfortable engaging with clinicians, healthcare leaders, and business stakeholders, and you have the ability to translate market insights into actionable business recommendations. Experience & Skills BSc or MSc in Life Sciences, Healthcare, Nursing, Pharmacy, Medicine, Business, Medical Technology A minimum of 5 years of clinical experience within Medical Oncology, Oncology Nursing, Oncology Pharmacy, Hematology/Oncology, or a related oncology specialty A minimum of 2 years of experience in business development, strategic marketing, product management, commercial strategy, market development, or a related function Strong understanding of Medical Oncology treatment pathways, clinical workflows, and healthcare systems Experience engaging with clinical stakeholders and key opinion leaders Strong analytical, communication, and stakeholder management skills Experience working in international and cross-functional environments Excellent command of English, spoken and written It is considered a strong advantage if you have experience within: Medical Oncology Oncology Drug Development Precision Medicine Biomarker-Driven Therapies Clinical Decision Support Solutions Oncology Informatics Healthcare Software Market Access and Reimbursement Exposure to pharmaceutical, biotechnology, healthcare software, oncology informatics, or medical technology companies is highly desirable.

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