Sr. Associate Scientist I

Bristol Myers SquibbSan Diego, CA
Onsite

About The Position

At RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, the mission is to develop transformative radiopharmaceutical therapies for cancer patients. The company blends the agile spirit of a biotech with the resources of a leading oncology innovator. RayzeBio, headquartered in San Diego, CA, was launched in late 2020 and acquired by BMS in 2024. It operates as a standalone entity, focusing on improving cancer survival through targeted radioisotopes. RayzeBio is developing innovative drugs against solid tumor targets, with its lead asset, RYZ101, in Phase 3 testing for GEP-NETs and earlier stage testing for SCLC. The company is led by an experienced entrepreneurial team aiming to be a global leader in radiopharmaceuticals. This laboratory-based role offers an opportunity to advance novel radiopharmaceutical therapies from the lab into clinical testing. The candidate will be responsible for developing, optimizing, and transferring biochemical and cell-based assays, including equilibrium binding assays, to support target validation, compound screening, and mechanism of action studies for various pipeline projects. A strong foundation in mammalian cell culture is essential. The ideal candidate is a critical thinker and technical problem solver who enjoys interdisciplinary drug discovery teams and is willing to work with radioactive isotopes.

Requirements

  • BS with 3–6 years of experience or MS with 2–4+ years of experience within Biology, Biochemistry, Molecular Biology, Pharmacology, or a related discipline with hands-on laboratory experience including cell culture and assay development.
  • Demonstrated expertise in mammalian cell culture with strong aseptic technique, and in vitro assay development and optimization, including equilibrium binding assays (saturation and competition formats).
  • Proficiency in techniques such as ELISA, MSD, flow cytometry, western blot, qPCR, and immunohistochemistry.
  • Experience with cell line engineering techniques (e.g., CRISPR, lentiviral transduction, stable transfection) for generating tool cell lines.
  • Proficiency with data analysis and visualization software (e.g., GraphPad Prism) for dose-response curve fitting and statistical evaluation of assay data.
  • Understanding of receptor-ligand binding theory and basic pharmacological concepts.
  • Excellent written and oral communication, presentation, and interpersonal skills with the ability to work in a fast-paced, dynamic, and collaborative environment.
  • Strong organizational skills and attention to detail.
  • Ability to work with radioisotopes with strict adherence to radiation safety protocols.

Nice To Haves

  • Prior experience working on drug discovery projects in an industrial or an academic setting is preferred.
  • Experience with assay transfer, qualification, and troubleshooting across laboratories is highly desirable.
  • Experience applying AI and computational tools to enhance data analysis, automate routine workflows, and support data-driven decision-making is desirable.

Responsibilities

  • Maintain and expand mammalian cell lines, including the generation of overexpressing and knockout lines, for use in screening and functional assays.
  • Validate reagents to characterize target expression and ensure cell line quality and consistency.
  • Develop, optimize, and run biochemical and cell-based assays to support the screening, characterization, and lead-identification of novel RPT agents.
  • Support assay transfer and qualification activities, including documentation of protocols, acceptance criteria, and reproducibility assessments across teams or sites.
  • Work with radioactivity in various assays in strict adherence to the radiation safety protocols.
  • Work under the guidance of project team leaders to support the overall biology screening and evaluation plan.
  • Work closely with chemists, DMPK, imaging, and in vivo teams to ensure implementation of screening funnel and appropriate prioritization of experiments.
  • Generate, organize, and maintain meticulous records on all conducted experiments.
  • Independently analyze and interpret data and present experimental plans and results at project team meetings, group meetings, and company meetings.
  • Actively contribute to the experimental design and planning efforts to help achieve project goals under tight timelines.
  • Collaborate with colleagues in other functional areas including translational research and chemistry.
  • Assist in laboratory operation management duties.

Benefits

  • Health Coverage: Medical, pharmacy, dental, and vision care.
  • Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
  • Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
  • Paid Time Off US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees).
  • Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays.
  • Unlimited paid sick time (based on eligibility).
  • Up to 2 paid volunteer days per year (based on eligibility).
  • Summer hours flexibility (based on eligibility).
  • Leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs.
  • Annual Global Shutdown between Christmas and New Years Day (for all global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year).

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What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Number of Employees

5,001-10,000 employees

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