Senior Research Associate, BMA

Senior Research Associate, BMA page is loaded## Senior Research Associate, BMAlocations: Norwood, Massachusetts: Clinical Developmenttime type: Full timeposted on: Posted Todayjob requisition id: R18319**The Role:**Moderna's Bioanalytical and Molecular Assay team is looking for a Senior Research Associate with strong hands-on experience in the regulated GLP/GCP bioanalytical LC-MS/MS area. The individual should have recent experiences in processing and analysis of a wide range of molecules such as lipids, biomarkers, proteins, and peptides. The role will support method development, validation, and sample analysis for the 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/colleagues, excellent work ethic, and setting the bar high are key values to thrive in our 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 Good Laboratory Practice (GLP), Good Clinical Practice (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 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* At Moderna, we are focused on delivering on our mission by enabling talent to thrive. For this role, we are currently unable to offer immigration sponsorship. Candidates must already hold work authorization in 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. That’s why 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 to support your unique needs* 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. 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 to learn more about our current opportunities.**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.**Equal Opportunities**Moderna is committed to equal employment opportunity 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. 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 an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.**Accommodations**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 accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation 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 team at .**Export Control Notice**This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicant’s ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license.#LI-CK1- #J-18808-Ljbffr

Created: 2025-09-21