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Eli Lilly and Company

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 fit
Core Competencies

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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

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Applicant 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 & technologies
PMP

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