Global Medical Director – Sleep Disorders, Neurology

Job not on LinkedIn

🕒 June 30

🏖️ New Jersey – Remote

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💵 $217k - $284.8k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

👻 Ghost score 6%

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Logo of Eisai US

Eisai US

1001 - 5000 employees

Founded 1995

💊 Pharmaceuticals

🏥 Healthcare

Pharmaceuticals • Healthcare

Eisai US is the United States arm of Eisai Inc. , a global pharmaceutical company focused on researching, developing, manufacturing and commercializing medicines — particularly in neurology (including Alzheimer’s disease) and oncology. With nearly 40 years of U. S. R&D and manufacturing presence, Eisai US runs clinical trials, patient support programs, community involvement and corporate responsibility initiatives under its “human health care” mission, and emphasizes a science-driven pipeline and collaborations to address areas of high medical need.

📋 Description

• Provide medical leadership for medical affairs strategy, planning and supportive tactics for sleep disorders. • Work with key stakeholders to develop and execute medical affairs strategy and priorities. • Provide strategic development, planning, implementation, and oversight of the global medical affairs plan. • Utilize expert medical/scientific knowledge in sleep disorders and orexin biology.

🎯 Requirements

• 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.

🏖️ Benefits

• Eisai Inc. Annual Incentive Plan • Eisai Inc. Long Term Incentive Plan • Employee benefit programs

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