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Senior Business Analyst

Job in Princeton, Mercer County, New Jersey, 08543, USA
Listing for: Bristol Myers Squibb
Full Time position
Listed on 2026-03-01
Job specializations:
  • IT/Tech
    Data Analyst
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

Working with Us

Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it.

You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more at

Summary

At Bristol Myers Squibb, we are inspired by a single vision—transforming patients' lives through science. Across oncology, hematology, immunology and cardiovascular disease, our colleagues advance innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

Position Overview

The Senior Business Analyst in the LIMS ELN and Entity Registration Platforms team will bridge scientific research needs and IT solutions, with a primary focus on Electronic Laboratory Notebooks/Laboratory Information Management Systems (ELN/LIMS) and the responsible adoption of Generative AI tools. This hands‑on role partners with researchers, lab personnel, and IT to gather requirements, design solutions, and ensure effective implementation and support of ELN/LIMS capabilities, instrument connectivity, and GenAI‑enabled workflows that improve data quality, speed of insight, and compliance.

Desired

Candidate Characteristics
  • Strong commitment to a career in technology with a passion for healthcare and impact on patients.
  • Proven experience with ELN/LIMS in biotech/pharma research labs.
  • Degree in Biological or Chemical Sciences with prior hands‑on research experience.
  • Knowledge of molecular biology, antibody discovery, protein chemistry/biochemistry workflows and data management.
  • Comfort translating scientific needs into system configurations, integrations, and training.
  • Ability to work collaboratively with scientists, IT colleagues, vendors, and contractors.
  • Demonstrated success operating within a matrixed organization and driving consensus.
  • Strong focus on user experience, change management, and adoption.
  • Excellent communication skills and agility to learn new tools and processes.
Key Responsibilities
  • Requirements Gathering:
    Collaborate with scientists and lab managers to understand experimental workflows; document user needs, process maps, and data standards for ELN/LIMS and GenAI use cases.
  • Solution Design:
    Partner with platform engineers and vendors to design configurations (schemas, registration models, templates, routing), integrations (APIs/webhooks/ETL), roles/permissions, and audit/traceability aligned with BMS standards.
  • GenAI Enablement:
    Identify high‑value GenAI opportunities (e.g., protocol drafting, experiment summarization, semantic search, assay troubleshooting assistants); define guardrails, evaluation, and privacy controls; support pilots through scale‑up.
  • Instrument & Data Connectivity:
    Coordinate instrument data capture, ensure metadata/FAIR practices, and support interoperability with analytics/warehouse environments.
  • Delivery & Support:
    Manage backlogs and Jira boards; write user stories and acceptance criteria; plan and script UAT; develop training materials and conduct structured end‑user training; provide post‑go‑live support.
  • Compliance & Quality:
    Partner with QA/Validation as applicable (e.g., 21 CFR Part 11, GxP/CLIA contexts), ensuring documentation, change control, and audit readiness.
  • Stakeholder & Vendor Management:
    Coordinate across Research, IT, Security, and vendors; contribute to roadmaps, SOWs, and service reviews to meet SLAs and continuous improvement goals.
Qualifications
  • Education:

    Bachelor’s or Master’s in Life Sciences (e.g., Molecular Biology, Biochemistry,…
Position Requirements
10+ Years work experience
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