Bavarian Nordic

• Integrate, validate and analyze data from CRM, digital platforms and other sources to create a unified and actionable view of customer activities • Define, standardize and monitor KPIs across CRM and digital platforms to ensure transparency, alignment and action • Develop, automate and maintain omnichannel and sales force effectiveness dashboards, and deliver campaign and engagement performance metrics across brands and geographies to assess performance and identify improvement areas • Conduct ad-hoc deep dives and root cause analyses to support tactical decision-making and strategic planning across markets and products • Ensure data quality, consistency and structure across internal and external sources • Act as the senior point of contact for all analytics topics related to field force, digital and omnichannel performance

Role Description The CMO Director is a key leadership role responsible for overseeing end-to-end operations with an assigned Contract Manufacturing Organization (CMO). This individual acts as the primary interface between Bavarian Nordic and the external partner, ensuring reliable supply, operational excellence, and strong cross-functional alignment across internal stakeholders, including Supply Chain, Quality, MSAT, Regulatory, Finance, and Procurement. This role requires a strategic, highly organized, and influential leader capable of managing complex external relationships, navigating technical and quality challenges, and driving performance within an outsourced manufacturing environment. Key Responsibilities - External Manufacturing Partner Management - Serve as the primary point of contact for the assigned CMO, managing day-to-day communication, governance meetings, and performance oversight. - Lead the execution of the external manufacturing strategy to ensure uninterrupted supply of commercial and/or clinical vaccine products. - Oversee contractual deliverables, service level expectations, and adherence to master service agreements (MSAs), quality agreements, and supply agreements. - Identify and resolve operational issues, escalating internally when needed to maintain supply continuity. - Cross-Functional Leadership - Coordinate with internal Supply Chain, Quality Assurance, Quality Control, Technical Operations, and Regulatory teams to ensure alignment of production plans, quality requirements, investigations, and change controls. - Drive scenario planning, risk mitigation, and issue resolution with internal SMEs to support CMO performance. - Partner with Finance and Procurement to manage budgets, review CMO invoices, support cost modeling, and contribute to contract negotiations. - Supply Planning & Operations Oversight - Ensure accurate forecast communication to CMOs and confirm capacity availability for commercial and development programs. - Monitor production schedules, batch execution, deviations, and release timelines to ensure adherence to supply plans. - Ensure production plans are executed in full and on time, with any risks proactively escalated. - Support inventory management activities, including material planning, work-in-process tracking, and lot disposition coordination. - Quality & Compliance Interface - Facilitate investigations, CAPAs, audits, and regulatory inspections involving the CMO. - Track operational and quality KPIs, ensuring performance meets internal expectations and industry standards. - Support change control processes, ensuring cross-functional impact assessments and timely implementation. - Technical & Process Support - Partner with Technical Operations to manage technical transfers, process improvements, validation activities, and troubleshooting at the CMO. - Ensure documentation, protocols, and reports generated by the CMO meet internal standards and regulatory requirements. - Strategic Contribution - Assist in strengthening the current ways of working and business processes used to manage external operations. - Contribute to long-range external manufacturing strategy, including capability assessments, risk evaluation, and network optimization. - Drive continuous improvement initiatives to enhance partnership effectiveness, reduce cost, and improve supply reliability. Qualifications - Required - Bachelor’s degree in Life Sciences, Engineering, Supply Chain, Business, or a related field. - 7+ years of biopharmaceutical, vaccine, or biologics manufacturing experience, with at least 3+ years in external manufacturing, CMO management, or similar supplier-facing roles. - Strong knowledge of GMP manufacturing, quality systems, and supply chain processes. - Demonstrated ability to lead in a matrixed environment and influence senior stakeholders. - Excellent communication, problem-solving, and relationship-management skills. - Experience managing complex projects and cross-functional workflows. - Preferred - Advanced degree (MBA or MS in a technical discipline). - Experience in vaccines, sterile manufacturing, or biological drug product operations. - Familiarity with tech transfer, scale-up, and process validation activities. - Experience working with mid-sized or fast-growing biopharma organizations. Benefits - Join a mission-driven global vaccine company at a pivotal stage of growth and evolution. - Opportunity to help shape innovative commercial programs, support public health initiatives, and contribute to how vaccines are accessed across healthcare channels. - Collaborative, entrepreneurial culture where cross-functional partnership, creativity, and impact are valued alongside scientific excellence. Company Description Bavarian Nordic is a global vaccine company focused on helping to protect lives through innovative vaccines, public health partnership, and expanded access to disease prevention. We work across emerging infectious diseases, travel health, and public health preparedness to help communities, healthcare providers, pharmacies, and health systems improve vaccine awareness, access, and delivery. With a growing commercial portfolio and strong global partnerships, Bavarian Nordic is evolving how vaccines are supported across healthcare ecosystems — combining scientific innovation with customer engagement, education, and public health impact.

Role Description The Channel Marketing Manager supports the development and execution of marketing strategies that drive vaccine adoption, access, and utilization within retail pharmacy and IDN channels. This role partners closely with brand marketing, sales, account management, and cross-functional teams to ensure channel-specific customers are equipped with effective tools, programs, and resources to strengthen vaccine recommendation and support vaccination delivery. The role focuses on activation programs that translate brand strategy into channel-specific execution, enabling pharmacists and IDN partners to effectively engage patients and increase vaccination rates. Key Responsibilities - Channel Strategy & Planning: - Support development of channel strategies aligned with vaccine brand priorities and commercial objectives - Contribute to annual planning and channel-specific tactical execution plans - Customer Activation & Engagement: - Design and implement retail pharmacy marketing programs that support pharmacist vaccine recommendations and point-of-care conversations, including pharmacist education and training tools, digital activation campaigns, seasonal vaccination and other appointment and traffic-driving initiatives - Design and implement IDN marketing programs that support population health initiatives, care gap closure, and vaccination protocols - Develop resources that enable account teams to effectively engage retail and IDN customers, including customer-specific toolkits, engagement materials, training resources, etc. - Partner with the brand teams to integrate channel-specific marketing activities with broader HCP and consumer engagement strategies - Ensure all materials are compliant with regulatory and legal standards - Channel Insights & Performance Analytics: - Monitor channel performance data and track key performance metrics including campaign effectiveness and retail engagement - In partnership with account management teams, drive insight generation on customer-specific operations, workflow, and patient dynamics to help identify opportunities to enhance channel engagement - Translate data/insight into actionable tactics to optimize marketing programs - Agency & Vendor Management: - Partner with external agencies to develop marketing materials and campaigns - Lead day-to-day execution and project management of channel marketing programs, coordinating timelines, agencies, and cross-functional stakeholders to ensure successful deployment across retail and IDN channels - Manage project timelines, budgets, and deliverables to ensure high-quality execution - Cross-Functional Collaboration: - Work closely with brand marketing, retail and IDN account management, commercial ops, field sales, medical affairs, legal and regulatory - Coordinate with Sales and Medical in deployment of channel-specific programs to achieve optimal customer experience with Bavarian Nordic and program effectiveness Qualifications - Bachelor’s degree required - 5+ years of experience in pharmaceutical, vaccine/biotech or healthcare marketing - Demonstrated experience in one or more of the following preferred: - Vaccine marketing - Brand marketing - Omnichannel campaigns - Customer engagement programs - Experience in working with retail pharmacy, health system or large provider group strongly preferred - Proven ability to lead cross-functional initiatives in complex commercial organizations and drive measurable commercial outcomes - Customer-centric mindset, strategic thinking and commercial acumen - Strong communication and project management skills - Ability to translate insights into scalable marketing programs - Analytical mindset with experience using data to drive decision-making - Strong cross-functional collaboration skills Benefits - Join a passionate, mission-driven global biotech committed to protecting lives - Collaborative culture - Flexible work environment - Opportunities for ongoing professional development and growth

Role Description Do you want to be part of a collaborative and supportive QA team and play a key role in ensuring the quality and safety of vaccines supplied to patients worldwide? At Bavarian Nordic, our vaccines make a real difference. We are seeking an experienced Senior QA Specialist to support in the ongoing oversight of a Contract Manufacturing Organization (CMO) operating under aseptic manufacturing conditions. This role is critical to ensuring compliance, product quality, and operational excellence across sterile fill-finish operations, including vial filling, labeling, and packaging activities. The ideal candidate will have deep expertise in aseptic GMP manufacturing environments, strong knowledge of sterile operations, and hands-on experience managing quality oversight of external manufacturing partners. As our new QA Specialist, you will take on a broad and impactful role, working directly with our affiliated CMOs and closely with stakeholders across the organization to ensure high quality standards within External Manufacturing production. Key Responsibilities - Ensuring CMOs maintain the highest levels of Quality standards conforming to cGMP and in conjunction with BN QAA - Support the Bavarian Nordic QPs to enable the release of the highest quality vaccines - Managing and resolving complex quality-related issues relating to aseptic operations including vial filling and labeling and secondary packing operations - Promoting a strong quality culture and driving continuous improvement initiatives across areas - Representing QA External Manufacturing in global and cross-organizational forums within Bavarian Nordic - Review and approve GMP documentation including: - Batch records - Deviations - CAPAs - Change controls - Validation protocols and reports - Ensure compliance with FDA, EU GMP, ICH, and applicable US regulatory requirements - Participate in risk assessments and investigations related to sterile manufacturing operations - Collaborate cross-functionally with Manufacturing, Supply Chain, Regulatory Affairs, and Technical Operations teams - Support technology transfers and process validation activities at external manufacturing sites - Lead or participate in internal and external GMP audits - Monitor quality metrics and drive continuous improvement initiatives with manufacturing partners - Serve as the primary QA liaison between the client and the CMO Qualifications - Bachelor’s degree in Chemistry, Biology, Pharmaceutical Sciences, Engineering, or related discipline - 10+ years of Quality Assurance experience in pharmaceutical or biotech manufacturing - 5+ years of strong experience with aseptic processing and sterile manufacturing environments is required - Demonstrated experience overseeing CMOs/CDMOs is a must - In-depth understanding of: - FDA cGMP regulations - EU GMP Annex 1 - Sterile fill-finish operations - Validation and contamination control strategies - Experience reviewing batch documentation and managing deviations/CAPAs - Excellent communication, organizational, and stakeholder management skills - Ability to travel periodically to manufacturing sites within the US or internationally as needed About the Team and Department You will join a competent and supportive QA External Manufacturing team, reporting directly to the Head of QA for External Manufacturing. The team currently consists of eight colleagues. The group is a mix of experienced QA professionals with DBS UDP and FDP experience, fostering collaboration, knowledge sharing, and continuous development. You will also become part of the wider External department, comprising approximately 40 employees across sites in Kvistgaard, Denmark, and Munich, Germany. The department is characterized by close cross-site collaboration, a strong quality mindset, and a shared commitment to delivering safe and compliant products to patients. Why Join Us Join a passionate, mission-driven global biotech committed to protecting lives. At Bavarian Nordic, you’ll find a collaborative culture, flexible work environment, and opportunities for ongoing professional development and growth. Bavarian Nordic is a global vaccine company with a mission to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America. Bavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. For more information, visit www.bavarian-nordic.com

Role Description The Key Account Manager, Infectious Disease – Central Region reports to the Director, Managed Markets and Infectious Disease. This field-based role is responsible for all facets of account management for assigned regional commercial and government accounts to attain key objectives for Bavarian Nordic products. This position will be responsible for creating and implementing short and long-term business plans working cross functionally with the National Account Management team and contracting to achieve Bavarian Nordic’s goals. - Increase Bavarian Nordic awareness in the US market and promote Bavarian Nordic products to achieve sales targets. - Assess and monitor product positioning within each targeted account, and when appropriate take action to increase or maintain open access to contracts and achieve goals. - Work cross functionally with contracting to monitor timelines for contract renewals and assist in developing contracts for key regional accounts. - Assist in developing and presenting sales presentations at the C-Suite level with key regional accounts. - Report progress in assigned accounts through business plan updates on a regular basis. - Serve as a subject matter expert on contracting and competitive landscape for key regional accounts. - Represent Bavarian Nordic at industry associations or national conferences as needed. Qualifications - Bachelor’s Degree from an accredited college or university. - 5+ years of professional industry/relevant experience; including strong knowledge of IDN contracting, state public health, federally qualified health centers, hospital contracting. - Vaccine experience preferred. - Ability to identify and build relationships with key decision-makers within assigned accounts. - Knowledge of CRM software and Microsoft Office Suite. - Exceptional communication skills that include verbal, written and presentation abilities. - Demonstrate effectiveness by operating in a field-based position at multiple levels. - Ability to accommodate 50% travel depending on Bavarian Nordic and/or customers’ needs. Benefits - Join a passionate, mission-driven global biotech committed to protecting lives. - Collaborative culture. - Flexible work environment. - Opportunities for ongoing professional development and growth. Company Description At Bavarian Nordic, we are dedicated to protecting lives and advancing global health through innovative vaccines. As a global leader in smallpox and mpox vaccines, our growing portfolio includes market-leading vaccines against rabies, chikungunya, cholera, and typhoid. Our mission is simple: to improve quality of life worldwide by preventing infectious diseases. We are headquartered in Denmark and have offices across Europe and North America.

• Managing Partner and Supplier Change Notifications • Performing Supplier Qualifications within the cGMP area • Conducting Internal Audits within the cGMP area • Processing and maintaining Quality Agreements • Supporting the development and continuous improvement of processes within the Audit & Inspection department • Acting as a key contact and subject matter expert within Audit & Inspection and GMP-related topics

Role Description The Key Account Manager, Infectious Disease reports to the Director, Managed Markets and Infectious Disease. This field-based role is responsible for all facets of account management for assigned regional commercial and government accounts to attain key objectives for Bavarian Nordic products. This position will be responsible for creating and implementing short and long-term business plans working cross functionally with the National Account Management team and contracting to achieve Bavarian Nordic’s goals. - Increase Bavarian Nordic awareness in the US market and promote Bavarian Nordic products to achieve sales targets - Assess and monitor product positioning within each targeted account, and when appropriate take action to increase or maintain open access to contracts and achieve goals - Work cross functionally with contracting to monitor timelines for contract renewals and assist in developing contracts for key regional accounts - Be able to assist in developing and presenting sales presentations at the C-Suite level with key regional accounts - Report progress in assigned accounts through business plan updates on a regular basis - Serve as a subject matter expert on contracting and competitive landscape for key regional accounts - Represent Bavarian Nordic at industry associations or national conferences as needed Qualifications - Bachelor’s Degree from an accredited college or university - 5+ years of professional industry/relevant experience; including strong knowledge of IDN contracting, state public health, federally qualified health centers, hospital contracting - Vaccine experience preferred - Ability to identify and build relationships with key decision-makers within assigned accounts - Knowledge of CRM software and Microsoft Office Suite - Exceptional communication skills that include verbal, written and presentation abilities - Demonstrate effectiveness by operating in a field-based position at multiple levels - Ability to accommodate 50% travel depending on Bavarian Nordic and/or customers’ needs Benefits - Join a passionate, mission-driven global biotech committed to protecting lives - Collaborative culture - Flexible work environment - Opportunities for ongoing professional development and growth Company Description Bavarian Nordic is a global vaccine company with a mission to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America. Bavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. For more information, visit www.bavarian-nordic.com

Protecting our tomorrow Job Title: Head of Clinical Operations & Biometrics Location: US Remote; East Coast Strongly Preferred Department: Research & Development Reports To: Senior Vice President, Research & Development Salary Range: $310k - $360k About Bavarian Nordic At Bavarian Nordic, we are dedicated to protecting lives and advancing global health through innovative vaccines. As a global leader in smallpox and mpox vaccines, our growing portfolio includes market-leading vaccines against rabies, chikungunya, cholera, and typhoid. Our mission is simple: to improve quality of life worldwide by preventing infectious diseases. We are headquartered in Denmark and have offices across Europe and North America. Position Overview The Head of Clinical Operations & Biometrics is accountable for planning, executing, and delivering Bavarian Nordic’s global clinical trial portfolio. This role oversees Clinical Operations, Data Management, Biostatistics, Medical Writing and Statistical Programming, ensuring high-quality, compliant, and efficient clinical development execution. Key Responsibilities - Develop and execute the overall clinical operations strategy across Phase I–IV trials - Build and lead a high-performing cross-functional organization covering Clinical Operations, Biometrics, Medical Writing and Vendor/CRO Oversight - Contribute to corporate development strategies and clinical trial design decisions - Ensure ICH-GCP compliance, and audit/inspection readiness - Ensure clinical trials meet targets for timeline, budget, quality, and enrolment - Own functional and study budgets, forecasting, and resource planning - Oversee and set up governance for CRO partnerships - Ensure robust data capture strategies, database design, cleaning processes, and database lock in alignment with study timelines - Oversee development, validation, and documentation of data standards (e.g., CDISC). - Oversee statistical design of trials, statistical analysis plans (SAPs), endpoint justification, and modelling - Ensure regulatory-grade statistical outputs and programming deliverables (TFLs, CSR outputs, submission datasets) - Build capabilities, develop talent, and mentor clinical operations and biometrics leaders and foster a culture of quality, accountability, and operational excellence Qualifications - Advanced degree in Life Sciences, Biostatistics, Public Health, Medicine, or related field (PhD, MSc, MPH, MD preferred) - 15+ years in clinical development within biotechnology or pharmaceutical industries. At least 5 years in a leadership position - Proven leadership of Clinical Operations and Biometrics functions - Experience managing global Phase I–III trials; vaccine or biologics experience highly preferred - Demonstrated success collaborating with regulatory authorities - Strong understanding of ICH-GCP. Knowledge of CDISC standards, and statistical methodologies is a plus - Strategic thinking with hands-on operational mindset - Ability to influence in matrix environments and manage external partners - High adaptability and comfort working in fast-paced biotechnology setting with multiple parallel priorities - Strong financial acumen with experience overseeing department and study budgets - Ability to travel globally up to 30% Why Join Us Join a passionate, mission-driven global biotech committed to protecting lives. At Bavarian Nordic, you’ll find a collaborative culture, flexible work environment, and opportunities for ongoing professional development and growth. Bavarian Nordic is a global vaccine company with a mission to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America. Bavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. For more information, visit www.bavarian-nordic.com #LI-MA1

Protecting our tomorrow Job Title: Head of Clinical Operations & Biometrics Location: US Remote; East Coast Strongly Preferred Department: Research & Development Reports To: Senior Vice President, Research & Development Salary Range: $310k - $360k About Bavarian Nordic At Bavarian Nordic, we are dedicated to protecting lives and advancing global health through innovative vaccines. As a global leader in smallpox and mpox vaccines, our growing portfolio includes market-leading vaccines against rabies, chikungunya, cholera, and typhoid. Our mission is simple: to improve quality of life worldwide by preventing infectious diseases. We are headquartered in Denmark and have offices across Europe and North America. Position Overview The Head of Clinical Operations & Biometrics is accountable for planning, executing, and delivering Bavarian Nordic’s global clinical trial portfolio. This role oversees Clinical Operations, Data Management, Biostatistics, Medical Writing and Statistical Programming, ensuring high-quality, compliant, and efficient clinical development execution. Key Responsibilities - Develop and execute the overall clinical operations strategy across Phase I–IV trials - Build and lead a high-performing cross-functional organization covering Clinical Operations, Biometrics, Medical Writing and Vendor/CRO Oversight - Contribute to corporate development strategies and clinical trial design decisions - Ensure ICH-GCP compliance, and audit/inspection readiness - Ensure clinical trials meet targets for timeline, budget, quality, and enrolment - Own functional and study budgets, forecasting, and resource planning - Oversee and set up governance for CRO partnerships - Ensure robust data capture strategies, database design, cleaning processes, and database lock in alignment with study timelines - Oversee development, validation, and documentation of data standards (e.g., CDISC). - Oversee statistical design of trials, statistical analysis plans (SAPs), endpoint justification, and modelling - Ensure regulatory-grade statistical outputs and programming deliverables (TFLs, CSR outputs, submission datasets) - Build capabilities, develop talent, and mentor clinical operations and biometrics leaders and foster a culture of quality, accountability, and operational excellence Qualifications - Advanced degree in Life Sciences, Biostatistics, Public Health, Medicine, or related field (PhD, MSc, MPH, MD preferred) - 15+ years in clinical development within biotechnology or pharmaceutical industries. At least 5 years in a leadership position - Proven leadership of Clinical Operations and Biometrics functions - Experience managing global Phase I–III trials; vaccine or biologics experience highly preferred - Demonstrated success collaborating with regulatory authorities - Strong understanding of ICH-GCP. Knowledge of CDISC standards, and statistical methodologies is a plus - Strategic thinking with hands-on operational mindset - Ability to influence in matrix environments and manage external partners - High adaptability and comfort working in fast-paced biotechnology setting with multiple parallel priorities - Strong financial acumen with experience overseeing department and study budgets - Ability to travel globally up to 30% Why Join Us Join a passionate, mission-driven global biotech committed to protecting lives. At Bavarian Nordic, you’ll find a collaborative culture, flexible work environment, and opportunities for ongoing professional development and growth. Bavarian Nordic is a global vaccine company with a mission to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America. Bavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. For more information, visit www.bavarian-nordic.com #LI-MA1

Protecting our tomorrow Job Title: Head of Medical Affairs & GCSP (Global Clinical Safety & Pharmacovigilance) Location: Remote – US East Coast Department: Research & Development Reports To: Senior VP of R&D Salary Range: $325k - $415k About Bavarian Nordic At Bavarian Nordic, we are dedicated to protecting lives and advancing global health through innovative vaccines. As a global leader in smallpox and mpox vaccines, our growing portfolio includes market-leading vaccines against rabies, chikungunya, cholera, and typhoid. Our mission is simple: to improve quality of life worldwide by preventing infectious diseases. We are headquartered in Denmark and have offices across Europe and North America. Position Overview We’re looking for an experienced Head of Medical Affairs & GCSP (Global Clinical Safety and Pharmacovigilance) providing medical leadership across GCSP, Epidemiology, Medical Affairs, and Medical & Process Compliance. You will guide patient safety and benefit–risk, shape evidence generation and medical governance, and partner closely with Regulatory, Clinical Development, Quality, CMC/Manufacturing, Commercial, and Market Access to ensure scientific rigor and aligned execution across the product lifecycle. The position reports to the SVP of R&D and should be based on the East Coast of the United States - global travel up to ~30% should be expected. Key Responsibilities - ·Lead and develop high-performing GCSP, Epidemiology, Medical Affairs, and Medical & Process Compliance teams, including people leadership, budgets, and talent development - ·Have oversight of the GCSP team and QPPV office - ·Set and execute global Medical Affairs strategy aligned to development milestones, regulatory interactions, and commercialization plans; ensure medical accuracy and balance across all external scientific content - ·Establish and scale regional medical networks to support local commercial teams, capture insights, and localize global strategies - ·Own medical information capabilities and responses to unsolicited medical inquiries - ·Drive late-stage and post-approval evidence generation, including RWE, observational, and epidemiological studies - ·Institute robust medical governance appropriate for company growth; chair and/or contribute to internal medical governance committees - ·Partner deeply with Clinical Development to inform future trials and label expansions; collaborate across Regulatory, Manufacturing/CMC, Quality, Commercial, and Market Access - ·Build strategic external relationships with key opinion leaders and public-health stakeholders Qualifications - Advanced degree is required, and an MD qualification is preferred for this role - Expertise in medical affairs, clinical safety, and global pharmacovigilance, with a strong foundation in immunology, epidemiology, and vaccine safety - 10+ years’ experience in a similar role - Strategic mindset and operational rigor to ensure patient safety and scientific excellence across the product lifecycle - 10+ years’ experience from a leadership role with both direct and indirect reports - Exceptional communicator who can translate complex medical and regulatory topics into clear, actionable guidance for both scientific and non-scientific stakeholders - As a trusted advisor to senior leadership, you provide confident counsel on medical strategy, compliance, and risk management - As a leader, you’re hands-on and people-focused—ready to coach, mentor, and elevate high-performing teams across regions—while orchestrating medical governance, evidence generation, and external collaborations with precision and credibility - Curious and data-driven; you monitor emerging trends, synthesize real-world evidence, and challenge assumptions to inform better decisions - Most importantly, you thrive in change; your judgment, integrity, and resilience help safeguard patient safety and support our transition from development to full commercialization in a fast-moving, life-science environment Why Join Us Join a passionate, mission-driven global biotech committed to protecting lives. At Bavarian Nordic, you’ll find a collaborative culture, flexible work environment, and opportunities for ongoing professional development and growth. Bavarian Nordic is a global vaccine company with a mission to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America. Bavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. For more information, visit www.bavarian-nordic.com #LI-MA1