We are a specialty vaccine company that develops, manufactures, and commercializes prophylactic vaccines for infectious diseases addressing unmet medical needs. We take a highly specialized and targeted approach, applying our deep expertise across multiple vaccine modalities, focused on providing either first-, best- or only-in-class vaccine solutions.
Responsibilities
The Global Medical Expert plays a pivotal role in shaping and executing the medical strategy for Valneva’s vaccine portfolio , with a strong focus on product launches and life cycle management. Acting as the Medical Affairs project lead for the Chikungunya program and contributing to the Shigella clinical program , this role ensures the integration of scientific excellence into brand strategies and medical education initiatives. The position involves cross-functional collaboration and stakeholder engagement at a global level to support access to vaccination and advance public health.
Medical Strategy & Leadership
- Develop and lead the medical strategy and Medical Plan for assigned products, aligned with overall Brand Strategy
- Serve as Medical Affairs project lead for the Chikungunya program, driving all pre-launch and supporting post-launch activities across markets
- Support Phase 2 clinical development activities for the Shigella vaccine, in coordination with Clinical Development and Regulatory teams
- Drive therapeutic area-specific publication plans and KOL engagement strategies for successful launches
Stakeholder & KOL Engagement
Identify and cultivate relationships with global KOLs, infectious disease specialists, and vaccine advocacy organizationsRepresent Valneva at international scientific meetings, advisory boards, and conferences to communicate key data and collect insightsDevelop and deliver scientific training and presentations for internal teams, HCPs, and external stakeholdersMedical Communication & Evidence Generation
Lead the development of scientific materials including white papers, FAQs, presentations, and publications for the Shigella programReview and provide medical input on regulatory submissions, Investigator’s Brochures (IBs), safety reports, and publicationsSupport data generation activities including External Grant Proposals (EGPs) and post-marketing researchLead the publication plan and support Investigator Initiated Studies (IIS) as neededCompliance & Medical Governance
Ensure medical accuracy and compliance of all external materials and regulatory documents (e.g. MSOP-0045)Safeguard adherence to internal codes of conduct and external regulations, including transparency, HCP engagement, and value transfer guidelinesContribute to the development and implementation of SOPs related to medical affairs activitiesEnsure high-quality, ethical scientific engagement at the intersection of medicine and commercializationRequirements
Advanced degree in Medicine (MD), Pharmacy (PharmD), or Life Sciences (PhD) , with expertise in relevant therapeutic areasMinimum of 5 years’ experience in developing and executing medical strategies in the pharmaceutical industryProven experience in clinical research and trial management , with the ability to effectively engage investigators and stakeholdersStrong presentation and scientific communication skills : capable of representing the company at medical, scientific, and public eventsSelf-motivated, proactive, and dynamic with a high level of independence and accountabilityExcellent interpersonal skills with the ability to quickly build relationships and influence stakeholdersStrong verbal and written communication abilities, with confidence in both one-on-one and group settingsDemonstrated leadership qualities with the ability to inspire, engage, and motivate cross-functional teamsHighly organized and detail-oriented with strong planning and coordination skillsCollaborative mindset with the ability to work effectively across departments and international teamsSolid decision-making and negotiation skills with strong problem-solving capabilitiesAnalytical mindset with proficiency in interpreting data and numerical informationAdaptable and resilient in dynamic environments, as well ass willingness to travelStrategic thinker with a solution-oriented approachFinancial acumen and resource management skills, including budget oversightBenefits
Working with Valneva means being part of a global biotech company with a clear vision to make a meaningful impact in the world . At Valneva, you can expect a dynamic and innovative work environment characterized by an open, appreciative company culture and exciting, impactful assignments . Enjoy the benefits of flat hierarchies , an international atmosphere, and regular company events that foster collaboration and connection.
Additionally, we offer :
Work Life Balance : Flexitime & Compensation daysFinancial perks : Performance-related bonus & Lunch vouchersLifelong learning : Unlimited access to LinkedIn Learning & German / English courses for freeHealth & Wellbeing : Free access to sports and fitness activities via myClubs & Office MassagesJoin us and shape the future of biotechnology!
Due to legal reasons we are obliged to disclose the minimum salary for this position, which is € 75.000 gross per year based on full-time employment. However our salaries are market oriented and in line with your qualifications and experience.
