The Role

Moderna is seeking an experienced Sr. Scientist to join our Bioanalytical and Molecular Assays Team. This role involves supporting biotransformation and regulated non-clinical studies and clinical trials. A successful candidate will provide hands on experiment, scientific and operational oversight of ADME, pharmacokinetic (PK), lipids, protein, and routine biomarker bioanalyses for Moderna mRNA based therapeutic pipeline.

Here’s What You’ll Do

• Support establishing LC-MS GLP/GCLP regulated capability and facilitate method development, validation, and sample analysis to support clinical and preclinical programs.
• Responsible for in-house GLP/GCLP infrastructure, hands on troubleshooting, systems and procedures to ensure adequate rigorous laboratory practices & regulatory requirements for bioanalytical activities assuring phase appropriate approach.
• Performing biotransformation experiments which include but not limited to metabolites ID, mass balance, protein binding, and ADME investigation for Moderna mRNA based therapeutic pipeline.
• Responsible for the design and execution of phase-appropriate clinical and preclinical analytical strategies including LC-MS based assays, immunoassay, quantitation of lipids and therapeutic proteins, lipid characterization, metabolite identification and PK/PD assay method development.
• Evaluate and review raw data and study analytical reports and assay validation reports, as appropriate, to ensure laboratories are performing analysis in compliance with current regulatory, industry, and Moderna standards and that data are of the required quality (regulatory and scientific).
• Assist in writing SOPs, regulatory submissions and in responding to regulatory queries when needed.
• Hands on experience in using various LIMS such as Thermo Watson, Lab Vantage, ELNs etc.
• Knowledge of AI application in regulated bioanalysis is preferred.
• Deep knowledge of 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 clinical bioanalysis to ensure practices are consistent with regulatory expectations.

Here’s What You’ll Bring To The Table

• Ph.D. in Chemistry, Biochemistry, Cell Biology, Immuno-oncology, Immunology, Cancer Biology, or related fields with a minimum of 5+ years of biotech/pharmaceutical industry experience. A B.S./M.S. with extensive bioanalytical experience will also be considered.
• Strong biotransformation experience. Familiar with HRMS and metabolite ID. Knowledge in ADME of therapeutic is a plus.
• Experience with RNA, LNP and cell therapy preferred.
• Track record with analytical development with deep expertise with bioanalytical LC-MS platform to support PK/TK, efficacy in clinical and preclinical toxicology studies.
• Experience with analytical method development across various platforms, (e.g. ELISA, MS, chromatography, etc.) including quantitation of lipids and therapeutic proteins in biological matrices, metabolite identification and impurity profiling.
• Experience managing third party assay laboratories, collaborations, and relevant bioanalytical vendors preferred.
• Strong knowledge of regulatory guidance such as BMV, M10 and similar.
• Demonstrated deeply understanding of global regulatory requirements including GLP, GCP and the clinical trial process.
• This role is expected to be in office 70% of the time with flexibility to work from home up to 30%.

Benefits

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.

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.

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 smoke-free, alcohol-free, and drug-free work environment.

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 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 an E-Verify Employer in the United States. 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 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 leavesandaccommodations@modernatx.com. (EEO Employer)