Senior Research Associate, BMA

The RoleModerna's Bioanalytical and Molecular Assay team is looking for a Senior Research Associate with hands-on experience in the regulated GLP/GCP bioanalytical LC-MS/MS area. The candidate should have recent experience in processing and analysis of molecules such as lipids, biomarkers, proteins, and peptides. The role will support method development, validation, and sample analysis for clinical studies applying LC/MS techniques. The candidate must thrive in a scientifically stimulating, fast-paced environment with high expectations. Ability to troubleshoot, collaborate with cross-functional teams, respect for peers, excellent work ethic, and high standards are key values for the team. Here/'s What You/'ll Do Develop, optimize, validate, and run bioanalytical LC/MS methods for quantitation of various types of molecules, particularly lipids, biomarkers, and proteins (peptides) Draft study plans, bioanalytical methods, and study reports Conduct bioanalytical assays following established protocols and SOPs, in compliance with GLP/GCP guidelines Coordinate with external CROs on method development, qualifications, and validations; review and approval SOWs, protocols, and reports Work closely with colleagues in Clinical Development as well as cross-functional groups Provide mass spectrometry support to scientists in Clinical Development, Platform, and other groups Stay abreast of literature, government guidelines, internal guidance on clinical trial conduct including GLP, GCP, internal SOPs and regulations and White Papers, as appropriate, for pre-clinical and clinical bioanalysis to ensure practices are consistent with regulatory expectations Here/'s What You/'ll Bring To The Table Bachelor’s degree with at least 5+ years of laboratory experience or MS with 3+ years of demonstrated hands-on experience with the development and validation of bioanalytical methods using LC-MS Hands-on experience with sample preparation/extraction techniques for various analytes from biological matrices such as SPE, LLE, protein precipitation. CRO experience is a plus Ability to develop and implement methods for high throughput or (semi-)automated data analysis (e.g. Hamilton/Tecan automation) Experience with working with Electronic Lab Notebooks Willingness to learn new concepts and challenge boundaries; adaptability to change Organization and attention to detail; ability to handle multiple projects in a fast-paced environment Strong interpersonal skills with an eagerness to work with and support colleagues in other departments Proven ability to develop and work independently and to collaborate cross-functionally to accomplish goals in a timely manner Note: At Moderna, we are currently unable to offer immigration sponsorship. Candidates must already hold work authorization in the US and be able to maintain that status without the need for future sponsorship. At Moderna, we believe that when you feel your best, you can do your best work. Our US benefits and global well-being resources are designed to support you—at work, at home, and everywhere in between. Best-in-class healthcare coverage, plus a suite of voluntary benefit programs A holistic approach to well-being, with access to fitness, mindfulness, and mental health support Lifestyle Spending Accounts to personalize your well-being journey Family planning and adoption benefits Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown Savings and investment opportunities Location-specific perks and extras 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. We are proud to be 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, visit /careers to learn more about our current opportunities. Our Working Model We believe in-person collaboration is critical to our success. Moderna champions the benefits of an in-office culture with a 70/30 work model, where 70% of time is in-office to foster innovation, teamwork, and mentorship. Equal Opportunities Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to 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 characteristic protected by law. Moderna is an E-Verify employer. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. Accommodations We are focused on attracting, retaining, developing, and advancing our employees. Moderna provides reasonable accommodations to qualified job applicants with disabilities. If you require an accommodation during the hiring process or to perform the essential functions of the position, contact . Export Control Notice This position may involve access to technology or data subject to U.S. export control laws (EAR). Employment is contingent upon the applicant’s ability to access export-controlled information in accordance with U.S. law. Only U.S. persons are eligible for this position, and Moderna cannot sponsor non-U.S. persons for an export control license. #J-18808-Ljbffr

Created: 2025-09-25