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Lilly-Lilly

ExploR&D Program Lead

Lilly-Lilly

. Serve as the single point of accountability for external collaboration projects spanning discovery, preclinical development, and clinical proof-of-concept .

Posted 10/8/2026full-timeUnited StatesSenior💰 $175,500 - $257,400 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in leading cross-functional collaboration projects within the pharmaceutical industry, focusing on program strategy, resource management, and budget oversight. Proven ability to synthesize complex scientific data and drive project execution while fostering high-performing teams and stakeholder alignment.

Highest-signal resume keywords
Project Management Certification (PMP)Cross-Functional Program LeadershipPharmaceutical Industry ExperienceScientific Data EvaluationExternal Collaboration Management

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
Program Strategy DevelopmentBudget ManagementWork Plan DevelopmentRisk/Benefit SynthesisClinical Data AnalysisTherapeutic Modalities KnowledgeProcess ImprovementResource ForecastingContract NegotiationStakeholder Consensus Building
Soft Skills
Exceptional Communication SkillsTeam LeadershipProblem SolvingInfluencing Senior StakeholdersAdaptability in Ambiguity
Tools & Technologies
Contemporary Project Management ToolsProject Management Methodologies
Certifications & Qualifications
Project Management Professional (PMP)
Industry Keywords
Pharmaceutical IndustryPreclinical DevelopmentClinical Proof-of-ConceptCell and Gene TherapiesAntibodiesPeptidesOligonucleotidesVaccinesSmall MoleculesTranslational Sciences

Tech Stack

Tools & technologies
PMP

About the role

Key responsibilities & impact
  • Serve as the single point of accountability for external collaboration projects spanning discovery, preclinical development, and clinical proof-of-concept
  • Define program strategy, forecast resource needs, and develop timelines and budgets
  • Lead large-scale, cross-functional programs with significant risk and complexity
  • Lead collaboration teams comprising ExploR&D personnel, LRL subject matter experts, and external biotech collaborators
  • Create high-performing teams and define program scope and executable work plans
  • Assist with contract negotiation and execute work plans after signature
  • Deliver projects on time, on budget, and within scope
  • Manage allocated budgets and resources for complex programs
  • Synthesize scientific literature, expert input, experimental data, and trial data to address key questions
  • Lead integration of cross-functional data, risk/benefit synthesis, strategic conclusions, and study designs
  • Serve as primary liaison between Lilly and external biotech collaborators
  • Anticipate and resolve barriers, align strategic plans, and drive collaboration success
  • Integrate input from regulators, vendors, customers, and other external stakeholders to guide program strategy
  • Contribute to diligence and workplan development
  • Identify process gaps and implement improvements to enhance portfolio delivery
  • Champion new tools, templates, and ways of working for project management excellence
  • Apply program insights across functions and geographic areas

Requirements

What you’ll need
  • Bachelor’s degree in biology or a STEM-related field
  • 5+ years of work experience in the pharmaceutical industry, including preclinical-translational sciences and/or clinical-stage drug development
  • Experience across therapeutic modalities such as cell and gene therapies, antibodies, peptides, oligonucleotides, vaccines, and small molecules
  • Recognized as an internal subject matter expert within a therapeutic or technical discipline
  • Deep scientific fluency across the drug discovery and development continuum
  • Ability to critically evaluate complex technical and clinical data
  • Experience with science-driven business decisions, asset strategy, portfolio management, and the pharmaceutical landscape
  • Ability to lead and influence teams and senior stakeholders in a matrixed environment
  • Exceptional verbal and written communication skills
  • Experience managing external collaborations and alliances
  • Ability to translate biotech partners’ needs into clear scopes of work, workplans, program execution, and deliverables
  • Ability to anticipate challenges, diagnose root causes, and build stakeholder consensus around creative solutions
  • Experience leading through ambiguity and uncertainty
  • Practical experience or certification in project management, such as PMP or equivalent
  • Experience with contemporary project management tools and methodologies
  • Proven ability to forecast resource needs, manage budgets, and deliver large-scale cross-functional programs on time, on budget, and within scope
  • Experience developing work plans and supporting contract negotiation
  • Demonstrated commitment to operational excellence and process improvement

Benefits

Comp & perks
  • Company bonus depending partly 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
  • Time off and leave of absence benefits
  • Well-being benefits, including employee assistance program, fitness benefits, and employee clubs and activities
  • Disability accommodation support during the application process