Lilly Posted September 24, 2026

Executive Medical Director - Physician -Early Clinical Development, Immunology

Boston, Massachusetts, United States of America FULL_TIME
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Lilly is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work, but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Position Summary

We are seeking a high-impact physician scientist and emerging industry leader to join our Immunology team as Executive Medical Director, Early Clinical Development. This role is designed for a clinical translational leader ready to step into enterprise influence, bridging the critical gap between discovery science and clinical application, driving the development of transformational medicines for patients with autoimmune and inflammatory diseases.

The successful candidate will serve as a  strategic and scientific leader, connecting discovery scientists, translational/biomarker experts, early clinical physicians, clinical pharmacologists, and late-stage clinicians to craft compelling therapeutic hypotheses and efficiently test them in early clinical development with line of sight to full development and approval.  This role requires strong matrix leadership, executive presence, and the ability to inspire high-performing teams, influencing cross-functional partners and advancing both internal and external portfolio opportunities to bring transformational treatments to patients with autoimmune and inflammatory diseases.

This position is ideal for a proven industry Director/Sr Director seeking broader leadership scope, enterprise visibility, and the opportunity to help build a dynamic and growing Immunology organization at Lilly.

Primary Responsibilities

Strategic Portfolio Leadership

Collaborate with discovery, translational medicine, and clinical teams to develop and refine therapeutic hypotheses for autoimmune and inflammatory diseases

Participate in prioritization of target and modality selection, integrating scientific rigor with clinical feasibility, unmet needs, and commercial potential, with particular attention to transformational potential of proposed programs

Evaluate and diligence external discovery and early clinical opportunities for potential partnerships or acquisitions

Provide scientific and clinical expertise to portfolio strategy to ensure a robust pipeline of transformational medicines in autoimmunity and inflammation

Act as a visible strategic leader within the immunology portfolio, influencing direction, investment decisions, and development priorities

Clinical Development Excellence

In collaboration with stakeholders, design early clinical studies that efficiently test therapeutic hypotheses

Collaborate with clinical pharmacology, biostatistics, regulatory affairs, operations, and other stakeholders to optimize study design and execution

Integrate translational endpoints and biomarker strategies to accelerate and maximize learning from early clinical studies and enable early decision-making

Contribute to regulatory interactions, including pre-IND, IND submissions, interactions to ex-US health authorities, as well as regulatory strategy development

Monitor patient safety and ensure compliance with GCP, FDA, ICH guidelines, and company policies

Drive innovative experimental medicine approaches and accelerate progression from first-in-human through proof-of-concept

Cross-Functional Leadership & Influence

Serve as scientific and medical expert across multiple therapeutic programs simultaneously

Lead early clinical strategy in cross-functional teams through matrix influence, aligning diverse stakeholders around common objectives

Facilitate decision-making processes across discovery, development, and commercial functions

Mentor and develop junior team members while building scientific capabilities across the organization

Operate as a culture-shaping leader who elevates performance, accountability, and collaboration across teams

External Partnerships & Scientific Exchange

Establish and maintain relationships with key opinion leaders and scientific experts in autoimmunity and inflammation

Represent Lilly at scientific conferences, advisory boards, and industry forums

Support business development activities through clinical scientific due diligence

As appropriate, identify, evaluate, and execute strategic partnerships with CROs, biotech companies, academic institutions, and research organizations to enable the discovery and early development portfolio and strategy

Enhance Lilly’s external scientific presence as a thought partner and collaborator in immunology innovation

Regulatory & Medical Affairs Support

Partner with regulatory colleagues on IND strategy, FDA interactions, and global development planning

Contribute medical expertise to regulatory submissions and agency communications

Support risk management planning and safety signal evaluation

Participate in data analysis, scientific publications, and medical communications

Help shape development strategy and regulatory positioning for early-stage immunology assets

Minimum Qualifications

Medical Doctor or Doctor of Osteopathy. Must be board eligible or certified in Rheumatology, Dermatology, Gastroenterology, Allergy/Immunology, or related specialty or have completed the comparable level of post-medical school clinical training relevant to the country of hiring. US trained physicians must have achieved board eligibility or certification. Physicians trained outside the US who are not US board eligible or certified may be hired directly for employment in the US at the discretion of the Chief Medical Officer.

Non-US trained physicians must have completed education and training at a medical school that meets the requirements of the Liaison Committee on Medical Education (LCME).

Preferred Qualifications

Minimum 3–5+ years of  pharmaceutical/biotechnology  industry experience with progression to Director or Sr Director responsibilities in early clinical development

PhD in Immunology, Molecular Biology, or related field strongly preferred

Demonstrated experience in early-phase clinical trial design and execution

Strong background in translational medicine and biomarker development or application

Track record of successful cross-functional collaboration and matrix leadership

Deep understanding of immunology, autoimmune disease pathophysiology, and current therapeutic landscape

Experience with novel immunomodulatory approaches (biologics, small molecules, cell therapies, genetic medicines)

Knowledge of regulatory requirements for early clinical development (IND strategy, FDA interactions, global regulatory agencies)

Familiarity with target  identification/prioritization  through causal human biology in areas of high unmet need, translational endpoints, biomarker strategies, precision medicine approaches, clinical pharmacology, and  pharmacokinetic/pharmacodynamic  modeling

Previous experience in autoimmune therapeutic areas (autoimmune, inflammatory, and allergic diseases within gastroenterology, rheumatology, dermatology, and respiratory specialties)

Publication record in peer-reviewed journals demonstrating scientific leadership

Experience with business development, licensing, or partnership activities

Previous regulatory interactions and FDA or other health authority meeting experience

Advanced degree or fellowship training in clinical research or pharmaceutical medicine

Experience with innovative experimental medicine trial designs and adaptive study approaches

Demonstrated ability to lead programs, influence strategy, and operate effectively in a fast-moving, high-visibility portfolio environment

Key Competencies

Scientific Leadership:

Ability to synthesize complex scientific data and translate into actionable clinical strategies

Strategic thinking and hypothesis generation capabilities

Critical evaluation of competitive landscape and market opportunities

Matrix Leadership & Influence:

Exceptional communication and interpersonal skills

Demonstrated ability to influence without authority and build consensus across diverse teams

Strong negotiation and conflict resolution capabilities

Cultural sensitivity and ability to work effectively in global environment

Executive presence with the ability to engage senior stakeholders

Execution Excellence:

Autonomous work style with strong project management capabilities

Results-oriented mindset with focus on patient impact and business objectives

Adaptability and resilience in fast-paced, evolving environment

Strong analytical and problem-solving skills

External Engagement:

Ability to build and maintain relationships with external scientific and clinical community

Strong presentation and public speaking capabilities

Professional network within  autoimmune/inflammatory  disease research community

Credibility as an emerging external scientific leader in immunology

Additional information and expectations

Travel: 25-40% domestic and international travel required

Location: Boston, San Diego, San Francisco, Indianapolis,

Reports to: head of Early Clinical Development, Immunology Discovery

Matrix relationships: Extensive collaboration across Discovery, Translational Medicine, Clinical Pharmacology, Quantitative Systems Pharmacology, Clinical Operations, Regulatory Affairs, and Search and Evaluation/Business Development

Opportunity to play a foundational leadership role in a rapidly expanding Lilly Immunology organization with strong executive sponsorship and pipeline momentum

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( https://careers.lilly.com/us/en/workplace-accommodation ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.  The anticipated wage for this position is

$265,500 - $389,400

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

#WeAreLilly

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( https://careers.lilly.com/us/en/workplace-accommodation ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.  The anticipated wage for this position is

$265,500 - $389,400

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

#WeAreLilly

Job details

Seniority
Executive/VP
Function
Clinical Development
Therapeutic area
Immunology
Location
Boston, Massachusetts, United States of America
Employment type
FULL_TIME

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 64 comparable Executive/VP Clinical Development roles across 21 biopharma companies.

64Comparable roles tracked
64Currently active
21Companies hiring similar roles
6Countries represented

Salary context

32 of 64 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $265,500/yr – $389,400/yr
Lowest disclosed · Senior Director Nonclinical Development · Mylan Inc. $151,000/yr – $314,000/yr
Peer group range $232,500 – $458,800 (median $301,850)

Where these roles are based

Top locations among the 64 comparable roles

United States57
United Kingdom3
Italy1
Switzerland1
Ireland1
India1

Seniority mix

64 of 64 peers have a known seniority level

Senior Director38
Executive/VP26

Therapeutic area mix

22 of 64 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology12
Immunology7
Gastroenterology1
Neuroscience1
Dermatology & Aesthetics1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

100%similar
Gilead Sciences, Inc. Foster City, United States Executive/VP
Same function Same therapeutic area Same seniority Same country
100%similar
Regeneron Pharmaceuticals, Inc (USA) Tarrytown, United States Executive/VP
Same function Same therapeutic area Same seniority Same country
100%similar
Vertex Pharmaceuticals Inc (US) Boston, United States Executive/VP
Same function Same therapeutic area Same seniority Same country
100%similar
AbbVie Executive/VP
Same function Same therapeutic area Same seniority Same country

Open in 2 locations

North Chicago, United StatesWaltham, United States
90%similar
Vertex Pharmaceuticals Inc (US) Seattle, United States Senior Director
Same function Same therapeutic area Adjacent seniority Same country
90%similar
Otsuka Pharmaceutical Development and Commercialization, Inc. Remote, United States Senior Director
Same function Same therapeutic area Adjacent seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

100%
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Function Therapeutic area Seniority Country
100%
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Function Therapeutic area Seniority Country
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Otsuka Pharmaceutical Development and Commercialization, Inc. · Remote, United States · Senior Director
Function Therapeutic area Adjacent seniority Country
60%
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Gilead Sciences, Inc. · Foster City, United States · Executive/VP
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.