Eisai Inc. Posted May 18, 2026

Global Medical Director, Sleep Disorders - Neurology Global Medical Affairs

Remote, United States Full time
Clinical Development Neuroscience Director

Eisai Inc. 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 Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai’s human health care (hhc) mission. We’re a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer’s disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference.   If this is your profile, we want to hear from you.

The Global Medical Director will provide medical leadership for medical affairs strategy, planning and supportive tactics for sleep disorders.  Under VP, Head of Neurology Global Medical Affairs, this role will be responsible for working with key stakeholders (clinical development team, regional medical affairs teams, global commercial/product franchise team, global value & access team as well as external KOLs) to develop and execute medical affairs strategy and priorities in the short and long term. This position provides strategic development, planning, implementation and oversight of the global medical affairs plan related to sleep disorders, for both approved and pipeline assets in the orexin class.

The Medical Director will utilize expert medical/scientific knowledge in sleep disorders and orexin biology to provide strategic input for the development of product strategies and liaise with external and internal stakeholders and strengthen Eisai’s medical reputation in the sleep disorders community.

Responsibilities:

Global Medical Strategy

Develop and continuously refine the global medical strategy and execution plan for sleep disorders across regions

Drive alignment with regional medical teams and clinical development team as well as global value & access team, ensuring adoption of: Best practices from early-launch countries

Key scientific insights and real-world learnings

Key publications into medical education

Lead the creation of: Global scientific narratives

Lifecycle management strategies (including RWE, publications)

Partner with regions to address unmet needs and optimize launch performance

Serve as a medical expert to provide direction on key internal business processes for approved and pipeline assets in the orexin class.

Work with scientific communication team to ensure Global IIS strategies in place and review IIS proposals in conjunction with the policies.

Pipeline Strategy –  (Late Phase Development)

Provide medical leadership for Phase 2 readout and Phase 3 readiness

Develop early and evolving scientific narratives to position pipeline compound(s) within the orexin class and broader sleep landscape by closely working with clinical development team

Contribute to Phase 3 clinical development plans, including: Endpoint relevance and differentiation strategy

Patient segmentation and unmet need positioning

Support internal decision-making through robust scientific interpretation of data

External Scientific Leadership & KOL Engagement

Identify, map, and develop relationships with global and regional sleep disorder KOLs

Lead and support Scientific exchange activities, advisory boards, Congress strategy and engagement

Ensure the organization is seen as a credible scientific leader in sleep disorders and orexin biology

Competitive Intelligence & Insights

Monitor and synthesize competitive landscape developments, including: Other orexin antagonists and agonists

Emerging mechanisms in sleep disorders

Translate insights into: Strategic recommendations

Differentiation opportunities for both assets

Collaborate cross-functionally to ensure consistent competitive positioning

Qualifications:

PhD, MD, or PharmD with 5+ years of relevant experience. Experience in Life Sciences industry preferred.

Advanced degree in sciences or related field with substantial experience in the pharma/biotech industry.

OR a combination of equivalent education, deep subject matter expertise in sleep disorders along with a broad overall experience.

Demonstrated experience in: Global medical roles with cross-regional responsibility

Product launch and lifecycle management

Late-phase development (Phase 2/3 involvement)

Prior experience in sleep disorders or orexin biology strongly preferred

Ability to translate complex scientific outputs into strategic recommendations in collaboration with clinical development/operation team as well as global value & access team.

Excellent communication and presentation skills

Demonstrated success in engaging external experts (KOLs)

Proven ability to lead in complex, matrixed, multinational environments with diverse stakeholders.

Deep understanding of the drug development lifecycle, evidence generation, and Medical Affairs governance.

Practical knowledge of FDA regulations/ICH guidelines regarding conduct of clinical studies in relevant therapeutic areas.

Bachelor's degree (Master's preferred) and 10+ years of relevant experience. Experience in Life Sciences industry preferred.

Skills:Communication & Cross-functional Influence, Critical Thinking & Business Agility, Healthcare Environment Dynamics, MA Strategic Thinking, Mentoring/ People Development, Resource Planning & Management, Technical Breadth (Medical Affairs)

Eisai Salary Transparency Language:

The annual base salary range for the Global Medical Director, Sleep Disorders - Neurology Global Medical Affairs is from :$217,000-$284,800

Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan & Eisai Inc. Long Term Incentive Plan.

Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills.

Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit https://careers.eisai.com/us/en/compensation-and-benefits .

Certain other benefits may be available for this position, please discuss any questions with your recruiter.

Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status.   Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans.

Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information:

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Job details

Seniority
Director
Function
Clinical Development
Therapeutic area
Neuroscience
Location
Remote, United States
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 247 comparable Director Clinical Development roles across 40 biopharma companies.

247Comparable roles tracked
233Currently active
40Companies hiring similar roles
17Countries represented

Salary context

126 of 247 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 Not listed on this posting
Lowest disclosed · Sr. Principal Associate - QA Clinical Trial Packaging Engineer · Lilly $65,250/yr – $169,400/yr
Peer group range $117,325 – $392,100 (median $264,000)

Where these roles are based

Top locations among the 247 comparable roles

United States184
United Kingdom14
India10
Spain9
Switzerland6
Poland6

+ 11 more countries

Seniority mix

247 of 247 peers have a known seniority level

Director180
Senior Director38
Principal29

Therapeutic area mix

94 of 247 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology45
Immunology18
Neuroscience11
Cardiovascular / CVRM7
Respiratory6
Ophthalmology3
Dermatology & Aesthetics2
Rare Disease2

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.

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Same function Same therapeutic area Same 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
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AstraZeneca · Boston, Massachusetts, United States of America · Director
Function Therapeutic area Seniority Country
100%
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Otsuka Pharmaceutical Development and Commercialization, Inc. · Remote, United States · Director
Function Therapeutic area Seniority Country
90%
Sr Director, Early Clinical Development, Neuroscience
E.R. Squibb & Sons,L.L.C. · Cambridge Crossing, United States · Senior Director
Function Therapeutic area Adjacent 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.