If you’re interested in this role, please apply in English and include an English version of your Resume/CV. The Role Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. Moderna is strengthening its international business services hub in Warsaw, supporting our growing global operations. We welcome professionals ready to help advance our mission and shape the future of mRNA medicines. In this role, you will be an individual contributor based in Warsaw, Poland, supporting global pharmacovigilance (PV) operations and Moderna’s expanding product portfolio. You will deliver timely, accurate assessment and compliant, high-quality triage, processing, and quality control of individual case safety reports (ICSRs) received from postmarketing and/or clinical trial sources. Working with Global Case Management Leads and vendors in a fast-paced, dynamic environment, you will help oversee workloads, strengthen training, and support global projects while maintaining the accuracy and confidentiality of safety information. Here’s What You’ll Do: Deliver accurate, compliant case intake and processing. Review source documents received from postmarketing and/or clinical trial sources to triage and book in ICSRs according to applicable regulations, guidelines, Standard Operating Procedures (SOPs), and company requirements. Maintain accurate case entry and attach and organize source documents and correspondence in the Argus database, supporting timely assessment and high-quality processing of adverse event reports. Apply rigorous quality control to automated intake and case management. Review cases received through Moderna’s intake tool to perform exception handling, conduct quality control of automated case data, and validate automated duplicate decisions. Manage invalid cases and support case deletion and merge activities. Coordinate across global stakeholders to resolve issues and manage workloads. Liaise with Global Case Management Leads and country specialists to escalate and resolve country-specific issues, including health authority download concerns. Collaborate with Global Case Management Leads and vendors to oversee workload management and support global projects. Keep safety-mailbox and translation activities running reliably. Oversee the Drug Safety mailbox, ensuring emails are triaged, acknowledged, reconciled, filed, and addressed daily. Coordinate translation activities during triage and book-in, and oversee the Translation mailbox to support the timely handling of safety information. Protect confidential information throughout the case-management process. Perform diligent redaction of source documents and outbound follow-up documentation containing protected health information (PHI). Manage the processing, translation, and redaction of safety information received from Moderna’s legal affiliates. Drive consistent follow-up and thorough reconciliation. Manage outbound postal follow-up requests for non-US regions and send electronic follow-up requests daily. Perform and oversee ICSR reconciliation with business and internal partners. Liaise cross-functionally to troubleshoot and optimize processes related to follow-up, redaction, and reconciliation. Strengthen training, continuous improvement, and inspection readiness. Work proactively with Global Case Management Leads and vendors to create and update training materials. Contribute to mentoring and training new colleagues as needed, support continuous improvement opportunities and inspection readiness activities, and contribute to presentations and discussions. Manage competing priorities with sound judgment. Perform multiple tasks simultaneously, prioritize competing requests and projects, and escalate issues as appropriate to maintain timely, accurate, and compliant delivery. Perform other tasks as assigned by global PV management. The key Moderna Mindsets you’ll need to succeed in the role: “We act with urgency; Action today compounds the lives saved tomorrow.” You will bring this mindset to timely case assessment, daily mailbox management, follow-up communication, and proactive escalation—moving safety information forward while maintaining the accuracy, confidentiality, and quality that compliant pharmacovigilance requires. “We digitize everywhere possible using the power of code to maximize our impact on patients.” You will apply a critical, quality-focused approach to automated intake, from checking case data to validating duplicate decisions. You will also explore opportunities to engage with Generative AI tools for training-material development and process improvement, with any use subject to appropriate approvals, data-privacy safeguards, applicable validation requirements, and human oversight. Here’s What You’ll Need (Basic Qualifications): University degree in Pharmacy/Medicine or other relevant life sciences discipline (Dentistry, Experimental Medicine, Microbiology, Veterinary, Biotechnology, Physiotherapy, Medical Biology or similar) Minimum 3 years of experience in drug safety/pharmacovigilance case processing Solid knowledge of ICH guidelines relevant to PV and of global PV regulations, including FDA, EMA, MHRA, PMDA, and Health Canada Argus safety database and other platforms MS Office suite, Excel, Powerpoint, SmartSheet, Visio Effective time management skills Excellent communication skills (verbal and writing); results oriented and strong attention to detail Proficiency in English (verbal and/or written) required due to global collaboration needs. Our Working Model  As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact. Moderna is a smoke-free, alcohol-free, and drug-free work environment. Pay & Benefits At Moderna, we believe that when you feel your best, you can do your best work. That’s why our benefits and well-being resources are designed to support you—at work, at home, and everywhere in between. Competitive healthcare, plus voluntary benefit programs to support your unique needs A holistic approach to well-being with access to fitness, mindfulness, and mental health support Family building benefits, including fertility, adoption, and surrogacy support Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown Savings and investments to help you plan for the future Location-specific perks and extras The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work. About Moderna Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.  By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities. We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply! Moderna is committed to equal opportunity in employment and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. We’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best. Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at [email protected]. - Our Mission and Vision At Moderna we are pioneering the development of a new class of drugs made of messenger RNA (mRNA). This novel drug platform builds on the discovery that modified mRNA can direct the body’s cellular machinery to produce nearly any protein of interest, from native proteins to antibodies and other entirely novel protein constructs that can have therapeutic activity inside and outside of cells. We have a clear mission to propel the field of mRNA science forward and deliver new medicines to patients and a unique vision for how to achieve this mission. Our Mission: To deliver on the promise of transformative messenger RNA (mRNA) science to bring new medicines to patients. Our Vision: To unlock the potential of mRNA by establishing an ecosystem of teams and partners that will work together to develop the broadest possible array of drugs, across diverse therapeutic areas and routes of administration, for serious diseases that are not treatable today. Third Party Staffing Agencies Moderna does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Moderna from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Moderna and do not obligate Moderna to pay fees if we hire from those resumes. Reasonable Accommodation Notice Moderna will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. Applicants with disabilities may be entitled to reasonable accommodation under the terms of the Americans with Disabilities Act and certain state or local laws. Please inform the company's personnel representative by calling 617-460-9346 or emailing [email protected] if you need assistance completing any forms or to otherwise participate in the application process. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. Return Home

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