Full-Time

Senior Director

Early Phase Chemistry

Posted on 11/24/2025

Lilly USA

Lilly USA

10,001+ employees

Global pharmaceutical company developing medicines

Compensation Overview

$151.5k - $222.2k/yr

+ Company Bonus

Indianapolis, IN, USA

In Person

Category
Biology & Biotech (2)
,
Requirements
  • Ph.D. in Organic Chemistry, Chemical Engineering, or related field with 15+ years of work experience OR an MS degree in Organic Chemistry, Chemical Engineering, or related field with 20+ years of equivalent work experience.
  • Minimum 10 years of CMC experience, specifically in early phase drug development required.
Responsibilities
  • Create a high-performance team culture that operates with clarity of roles, responsibilities, and expectations for both individuals and the team.
  • Ensure safety of employees and facilities, and robust safety programs and procedures are in place.
  • Recruit, develop and grow the next generation of leaders.
  • Actively coach and mentor scientists of all levels across the organization.
  • Foster an environment of collaboration and innovation within the early phase chemistry group and larger Lilly Research Labs organization
  • Deliver Early Phase material to meet toxicologic and clinical milestones.
  • Develop a global network of active pharmaceutical ingredient, starting materials, and custom intermediates at CDMOs
  • Build and drive the strategy for internal effort Small Molecules at the Medicine Foundry.
  • Provide strategic guidance including synthetic, formulation and manufacturing strategies; this will include integration and application of new technologies.
  • Partner with cross-functional teams to ensure seamless integration of CMC development activities with other areas including discovery, toxicology, clinical development.
  • Accelerate discovery and development learnings through Lilly Research Labs partnership and pre-candidate selection to clinical supply material generation.
  • Integrate new technology and partnerships to increase Early Phase capabilities and efficiencies.
  • Drive successful synthetic route selection and route scouting efforts from Discovery to Ph II, internally and at partner CDMOs
  • Ability to communicate complex technical strategies with clarity
  • Actively manage internal and external resources to drive early phase drug development
  • Have a deep understanding of the portfolio, project objectives, and how the technical programs and people are poised to deliver on those objectives
  • Provide strategic leadership of early phase chemistry and broader SMDD chemistry goals and objectives.
  • Communicate and support execution of SMDD strategy.
  • Effectively evaluates organizational strengths and needs and drive appropriate changes.
  • Identify opportunities for continual improvement projects that optimize business processes.
Desired Qualifications
  • Proven track record of building and leading high performing teams
  • Track record of driving effective culture change
  • Excellent communication (written and verbal)
  • Exceptional external network and networking skills
  • Exceptional teamwork/Interpersonal/Leadership/Vision
  • Previous experience leading large teams
  • Expertise in project planning/organization/management
  • Talent assessment and recruiting
  • Knowledge of drug development life cycle
  • Patent filings and intellectual experience
  • Travel: 0 to 10%
  • Position Location: Indianapolis, IN

Lilly is a global pharmaceutical company that discovers, develops, and sells prescription medicines to improve health outcomes. It grows its portfolio through extensive research and development, then manufactures and distributes drugs worldwide to healthcare providers who prescribe them to patients. Lilly’s products span diabetes, cancer, immunology, pain management, and other serious conditions, including diabetes treatments tirzepatide and dulaglutide. The company emphasizes safety, efficacy, and ethical practices, and protects its products from counterfeiting while partnering with organizations such as Team USA. Its approach relies on rigorous R&D, strong manufacturing, and a global distribution network to bring medicines to patients. Lilly’s goal is to help people live better lives by delivering reliable medical solutions through a global, ethical, and quality-focused operation.

Company Size

10,001+

Company Stage

IPO

Headquarters

Indianapolis, Indiana

Founded

1876

Simplify Jobs

Simplify's Take

What believers are saying

  • Medicare's GLP-1 Bridge can broaden access to Mounjaro and Zepbound.
  • CVS restored Zepbound coverage and added Foundayo across major formularies.
  • Lilly can redeploy capital from Germany toward U.S. manufacturing expansion.

What critics are saying

  • Medicare's bridge program compresses pricing and shifts volume from premium channels.
  • CVS can re-prefer Wegovy or exclude obesity drugs entirely on sponsor opt-outs.
  • Lilly's tirzepatide concentration makes any safety, supply, or pricing shock severe.

What makes Lilly USA unique

  • Lilly dominates diabetes and obesity with Mounjaro and Zepbound, driving 56% revenue.
  • The company pairs blockbuster commercialization with deep R&D and global manufacturing scale.
  • Recent acquisitions add vaccines and non-viral genetic medicine platforms beyond GLP-1s.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

Life Insurance

401(k) Retirement Plan

401(k) Company Match

Paid Vacation

Flexible Work Hours

Wellness Program

Growth & Insights and Company News

Headcount

6 month growth

-2%

1 year growth

-5%

2 year growth

-5%
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The FDA is requesting additional safety data from Eli Lilly for its weight loss pill Foundayo, including information on potential heart and liver problems, according to the approval letter published Tuesday. The agency wants more data on risks including heart attacks, strokes, drug-induced liver injuries and delayed stomach emptying. Foundayo, approved this month under a fast-track pilot programme, is the second oral GLP-1 to reach market after Novo Nordisk's Wegovy pill. The FDA is also asking Lilly to collect thyroid cancer risk data for at least 15 years. The requests are considered routine for newly approved drugs, particularly for orforglipron, Foundayo's active ingredient, which has less safety data than older GLP-1s. Lilly must also establish registries tracking children with obesity and pregnancy outcomes.

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