Senior Scientist, Global Nonclinical and Scientific Documentation
Share
Job Location:
New Brunswick, NJ - USA
Monthly Salary:
Not Disclosed
Posted on:
14 hours ago
Vacancies:
1 Vacancy
Job Summary
Working with Us
Challenging. Meaningful. Life-changing. Those arent 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. Youll 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: Summary
This Senior Scientist position is for a computationally minded individual with a strong understanding of biology and drug development to work within the Global Nonclinical and Scientific Documentation (GNSD) group. GNSD partners with nonclinical scientists across pharmacology drug metabolism and pharmacokinetics (DMPK) bioanalysis (BA) and toxicology to assist in the preparation generation and review of nonclinical study reports and global regulatory-facing documents. GNSD is an essential component for all drug development programs within the BMS pipeline from candidate nomination to global approval across all therapeutic areas and modalities.
In support of our remit we are seeking a talented individual with a strong background in both nonclinical regulatory submissions (in support of pharmacology DMPK BA and toxicology SMEs) and large language models (LLMs) and software solutions. This individual will be responsible for bridging our current ways of working with the future of document generation supporting todays nonclinical documentation needs while actively leading the transformation toward next-generation AI-driven workflows. The role will apply modern AI to the creation of high-quality summary documents for inclusion in submissions to global health authorities. The individual will work as support for nonclincial SMEs on drug development programs and closely with internal research informatics partners to optimize and support internally built BMS tools. They will thoughtfully integrate best-in-class solutions into existing workflows while driving adoption across the organization. The ideal candidate is project-focused organized communicative and fluent across both life and computational sciences. This position offers an exciting opportunity to be at the center of BMSs mission to rewire and modernize the drug development process as we bring novel therapeutics to patients.
Key Responsibilities
- Support nonclinical SMEs partnering in the authoring review and project managing of high-quality nonclinical study reports and regulatory-facing documents for global health authority submissions.
- Represent GNSD on strategic workstreams to institute the use of AI within BMS
- Develop and optimize AI tools for nonclinical scientists to assist in the interpretation reporting and presentation of scientific data across pharmacology DMPK Bioanalytical and toxicology
- Champion the implementation and adoption of AI tools by the BMS nonclinical scientific community
- Partner with internal and external stakeholders to evaluate pilot and integrate emerging technologies into nonclinical documentation workflows
About Company
Bristol-Myers Squibb is a global biopharmaceutical company focused on discovering, developing and delivering innovative medicines for patients with serious diseases. Our medicines are helping millions of patients around the world in disease areas such as oncology, cardiovascular, immu ... View more
