Senior Scientist, Global Nonclinical and Scientific Documentation
Bristol Myers Squibb
2 days ago
Remote friendly (Brisbane, CA)
United States
Operations
Position Summary
Senior Scientist (computationally minded; strong understanding of biology and drug development) within the Global Nonclinical and Scientific Documentation (GNSD) group.
Key Responsibilities
- Partner with nonclinical SME’s in the authoring, review, and project management 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 to help nonclinical scientists interpret, report, and present scientific data across pharmacology, DMPK, bioanalytical, and toxicology.
- Champion 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.
Qualifications & Experience
- Education in life sciences and/or computational sciences.
- Bachelor’s preferred with minimum 7 years relevant experience, or advanced degree with minimum 5 years relevant experience.
- Strong appreciation of drug development sciences (pharmacology, DMPK, bioanalysis, and/or toxicology).
- Demonstrated expertise using AI/ML tools for handling and/or interpreting large sets of numerical and scientific data.
- Strong project management skills; ability to prioritize and deliver in a fast-paced environment.
- Experience with regulatory documents and global health authority submissions (e.g., IND, NDA, BLA, or CTD/eCTD format).
Senior Scientist (computationally minded; strong understanding of biology and drug development) within the Global Nonclinical and Scientific Documentation (GNSD) group.
Key Responsibilities
- Partner with nonclinical SME’s in the authoring, review, and project management 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 to help nonclinical scientists interpret, report, and present scientific data across pharmacology, DMPK, bioanalytical, and toxicology.
- Champion 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.
Qualifications & Experience
- Education in life sciences and/or computational sciences.
- Bachelor’s preferred with minimum 7 years relevant experience, or advanced degree with minimum 5 years relevant experience.
- Strong appreciation of drug development sciences (pharmacology, DMPK, bioanalysis, and/or toxicology).
- Demonstrated expertise using AI/ML tools for handling and/or interpreting large sets of numerical and scientific data.
- Strong project management skills; ability to prioritize and deliver in a fast-paced environment.
- Experience with regulatory documents and global health authority submissions (e.g., IND, NDA, BLA, or CTD/eCTD format).