Senior Research Associate or Associate Scientist, Translational Medicine

Responsibilities : With guidance from a Senior Scientist, Translational Medicine, perform assays on clinical samples and potentially pre-clinical samples. Perform qualified or validated molecular based assays (Luminex, dPCR, MSD, ELISA, etc.) on clinical samples to inform on cell product persistence and efficacy in humans. Participate in generating, qualifying, and validating GLP-like assays and contributing to the development of corresponding SOPs. Interfacing heavily with the electronic lab notebook (eLN) system and sample management system; accurately capturing data in a timely manner, ensuring data integrity and protocol compliance using an eLN. Maintain GDP-compliant and detailed records for clinical sample lifecycle (receipt, usage, inventory, etc.). Involvement in clinical sample accessioning with close attention to metadata entry. Opportunities to learn and perform cell based assays such as flow cytometry and cell killing assays. Manage multiple internal projects / workstreams simultaneously. Performing lab associated tasks in accordance with GLP and Cabaletta Bio lab safety policies and SOPs. General maintenance of laboratory space and contribution to weekly activities. Required

Qualifications : MS degree in Biology, Immunology, Engineering or related field or Bachelor’s degree with 2+ years of experience in an academic laboratory or the biotechnology industry is required. Experience with molecular based assays such as ELISA’s, MSD, Luminex, and/or dPCR platforms. Significant lab experience including aseptic technique, mammalian cell culture, and DNA extraction. Must be able to follow SOPs and follow good documentation practices. Must be highly organized and efficient, able to work independently. Strong problem-solving skills are preferred. Must be able to communicate clearly verbally and in writing. Must have a desire to be part of a growing organization that uses cutting-edge science. Strong team orientation and passion for continuous self-development. Comfortable in a fast-paced small company environment and able to adjust workload based upon changing priorities. Preferred

Qualifications : Experience in protocol design, qualification, and SOP generation. Experience with qPCR/dPCR platforms. Experience with autoantibody evaluation assays. Experience with clinical sample handling and inventory management is strongly preferred. Experience troubleshooting, qualifying, or validating molecular based assays. Experience in the biotechnology industry or in a startup industrial setting. Previous experience with GLP/GCP & ICH regulations. Prior use of an electronic laboratory notebook system; involvement in system development is a plus. Our name – Cabaletta – is derived from the operatic term that represents a rapid, repetitive, and technically challenging section of an operatic aria, designed to showcase the skills of the lead singer. Analogously, Cabaletta Bio strives to achieve rapid and repetitive product development, building on our indication prioritization and biologic platform that targets the driver of specific autoimmune diseases without the need for long-term immunosuppression. For more information, please visit https://www.cabalettabio.com/join-our-crew Our most important asset is our people, and we offer competitive

benefits, PTO, and stock option plans. Cabaletta Bio is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability, protected veteran status or any other basis protected by applicable law. Cabaletta Bio, Inc. does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with Cabaletta, a Master Services Agreement (MSA) must be executed and confirmed prior to submitting any information relating to a potential candidate. Without a signed MSA, Cabaletta shall not be responsible to any individual or entity for any payment relating to any form of fee or

compensation. And, if a resume or candidate is submitted by a recruiter, an employment agency, or a staffing firm without a fully executed MSA, Cabaletta has the unrestricted right to pursue and hire any of those candidate(s) without any legal or financial responsibility to the recruiter, agency, and/or firm. LI-ONSITE Apply for this job First name Last name Email address Location Phone number Resume Attach resume Attach another file Attach file Add another What are your salary

requirements? Are you authorized to work in the United States? Yes No Will you now or in the future require sponsorship for employment visa status (e.g. H-1B status)? Yes No Do you have experience with molecular based assays such as ELISA’s, MSD, Luminex? Do you have experience with qPCR/dPCR platforms? Are you familiar with GLP/GCP & ICH regulations? Linkedin url Should be {http://www.linkedin.com/pub/[member-name/]x/y/z} or {http://www.linkedin.com/in/string} © 2014-2026 TriNet Group, Inc. All rights reserved. Privacy Policy

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