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Principal Scientist – ADME
Eli Lilly and Company. Advance Lilly's ADME discovery portfolio through bioanalytical, drug-drug interaction (DDI), and project oversight activities .
Posted 10/8/2026full-timeIndianapolis • Massachusetts • United StatesLead💰 $69,000 - $195,800 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in bioanalytical studies, drug-drug interaction oversight, and vendor management within pharmaceutical operations. Proficient in project management and data quality assurance, with a strong focus on compliance and operational efficiency.
Highest-signal resume keywords
Bioanalytical Study OversightVendor ManagementProject Management Certification (PMP)LC-MS Bioanalytical PlatformsData Quality Assurance
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
BioanalysisDrug Metabolism and Pharmacokinetics (DMPK)ADME StudiesStudy Data ReviewBudget ManagementInvoice ReconciliationPerformance MonitoringProcess ImprovementScientific DocumentationCross-Functional Collaboration
Soft Skills
Problem-SolvingOrganizationFollow-ThroughWritten CommunicationVerbal Communication
Tools & Technologies
SmartsheetSciQuerySAP FioriAnalyst SoftwareWatson SoftwareAI ToolsWorkflow Automation
Certifications & Qualifications
Project Management Certification (PMP)
Industry Keywords
CRO OversightVendor RelationshipsOperational MetricsScientific ReviewsCompliance
Tech Stack
Tools & technologiesPMP
About the role
Key responsibilities & impact- Advance Lilly's ADME discovery portfolio through bioanalytical, drug-drug interaction (DDI), and project oversight activities
- Lead bioanalytical and DDI studies with external research partners
- Track study progress in Smartsheet and resolve issues
- Manage study requests and vendor deliverables from intake through quality review
- Review assay performance, data packages, deviations, and study reports for scientific and quality standards
- Conduct annual scientific reviews of assigned vendors
- Escalate technical or data-quality concerns and drive corrective action with scientists and quality teams
- Ensure studies and contracts are delivered on time, within budget, and to scope
- Reconcile vendor invoices and commitments against actual utilization
- Report spend and operational metrics to stakeholders
- Partner with quality, finance, project leadership, and internal scientific teams on vendor oversight and compliance
- Apply approved AI and automation tools to improve data review, reporting, efficiency, and data quality
- Support vendor governance, performance reviews, and contract renewals
- Build vendor relationships and provide operational summaries and presentations to internal stakeholders
Requirements
What you’ll need- Bachelor's degree, preferably in a scientific field (e.g., chemistry, biochemistry, biology, pharmaceutical sciences)
- 7+ years of experience in a laboratory, CRO, or pharmaceutical operations setting, including vendor oversight
- Experience reviewing bioanalytical, DMPK, or DDI study data and reports, and communicating concerns to vendors and internal partners
- Advanced degree in a scientific field preferred
- Experience in ADME, bioanalysis, or drug metabolism and pharmacokinetics (DMPK), including in vitro and in vivo study types preferred
- Familiarity with LC-MS bioanalytical platforms and software, such as Analyst and Watson, and CRO data delivery workflows preferred
- Experience with CRO oversight and sponsor-vendor interactions, including budget and invoice management, performance monitoring, and process improvement preferred
- Project management certification, such as PMP, and demonstrated ability to manage multiple concurrent projects/programs to meet deliverable timelines preferred
- Proficiency with SciQuery, SAP Fiori, and Smartsheet, and familiarity with RRL data loading and enterprise scientific data platforms preferred
- Familiarity with AI and automation tools, such as generative AI assistants and workflow automation, preferred
- Ability to produce high-quality written documentation including SOPs, job aids, reports, and executive-level summaries
- Excellent problem-solving, organization, follow-through, written and verbal communication, and cross-functional collaboration skills
- Up to 10% travel
Benefits
Comp & perks- Company bonus depending, in part, on company and individual performance
- Company-sponsored 401(k)
- Pension
- Vacation benefits
- Medical, dental, vision, and prescription drug benefits
- Flexible benefits, including healthcare and/or dependent day care flexible spending accounts
- Life insurance and death benefits
- Certain time off and leave of absence benefits
- Well-being benefits, including employee assistance program, fitness benefits, and employee clubs and activities
- Employee resource groups and support networks