
10,000+ employees
đź’Š Pharmaceuticals
🏥 Healthcare
🧬 Biotechnology
đź’° $6.5M Post-IPO Debt - Eli Lilly on 2024-02
Pharmaceuticals • Healthcare • Biotechnology
Eli Lilly and Company is a multinational pharmaceutical company that researches, develops, manufactures, and markets prescription medicines across multiple therapeutic areas including diabetes, oncology, immunology, neuroscience, and pain. Headquartered in Indianapolis, Indiana, Lilly is known for its extensive R&D, clinical development, and global commercialization of biologic and small-molecule drugs. The company focuses on drug discovery, clinical trials, regulatory approvals, and large-scale pharmaceutical manufacturing and distribution.
🔥 17 hours ago
🇺🇸 United States – Remote
đź’µ $177k - $338.8k / year
⏰ Full Time
đźź Senior
đź‘” Director
đź‘» Ghost score 0%
Improve your chances of getting an interview by checking your resume score before you apply.

10,000+ employees
đź’Š Pharmaceuticals
🏥 Healthcare
🧬 Biotechnology
đź’° $6.5M Post-IPO Debt - Eli Lilly on 2024-02
Pharmaceuticals • Healthcare • Biotechnology
Eli Lilly and Company is a multinational pharmaceutical company that researches, develops, manufactures, and markets prescription medicines across multiple therapeutic areas including diabetes, oncology, immunology, neuroscience, and pain. Headquartered in Indianapolis, Indiana, Lilly is known for its extensive R&D, clinical development, and global commercialization of biologic and small-molecule drugs. The company focuses on drug discovery, clinical trials, regulatory approvals, and large-scale pharmaceutical manufacturing and distribution.
• Serve as the Global Medical Affairs Lead for Centessa's lead orexin receptor 2 agonist program • Develop and execute the global medical strategy across the product lifecycle • Lead global medical affairs strategy and tactical execution for cleminorexton • Serve as a core member of the cross-functional asset team • Align medical strategy with corporate objectives, clinical development milestones, and commercialization plans • Establish long-range medical affairs planning for regulatory approvals, launch readiness, and lifecycle management • Identify emerging scientific opportunities, evidence gaps, and stakeholder needs • Lead medical launch preparedness across major global markets • Partner with commercial, market access, HEOR, regulatory affairs, and regional medical teams on integrated launch strategies • Oversee launch deliverables including scientific platforms, training content, medical information resources, publications, congress activities, and insights generation • Support pre-launch and launch planning, including global payer engagement strategies and value communication • Build and maintain relationships with global key opinion leaders, investigators, professional societies, and patient advocacy organizations • Lead scientific advisory boards, expert consultations, and insight-gathering initiatives • Represent Centessa at scientific congresses and industry meetings • Serve as a scientific ambassador and subject matter expert for orexin biology and sleep-wake disorders • Act as a strategic partner to commercial, market access, HEOR, regulatory, clinical development, patient advocacy, and corporate affairs • Contribute medical expertise to brand strategy, payer engagement, disease-state education, and scientific communications • Partner on scientific platforms, publication strategies, educational programs, and medical training • Provide medical review and guidance for externally facing scientific materials • Report to the Head of Medical Affairs and partner with senior leadership
• Advanced scientific or clinical degree (MD, PharmD, or PhD) • Minimum 10 years of Medical Affairs leadership experience; 5 years global experience preferred • Experience in neuroscience, sleep medicine, neurology, psychiatry, or rare disease • Demonstrated experience leading at least one successful global product launch; North America, Europe, and Asia-Pacific markets highly preferred • Experience serving as a global medical lead for late-stage development or commercial products • Strong understanding of global medical affairs, evidence generation, payer evidence requirements, and commercialization readiness • Proven ability to drive strategy in a matrix environment • Proven track record of collaborating closely with commercial, market access, HEOR, regulatory affairs, and clinical development organizations • Exceptional communication, presentation, and stakeholder management skills • Based in the US • Occasional travel (~20%)
• 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
Apply Now🔥 18 hours ago
Senior Director building Definium’s field organization for DT120 site activation and reimbursement. Advancing commercial access to psychedelic-based psychiatric treatments.
đź•’ Yesterday
Senior Director expanding WellRight’s corporate wellness platform through broker and benefit consultant relationships. Driving consultant outreach, strategic partnerships, pipeline growth, and sales conversion.
🇺🇸 United States – Remote
đź’µ $175k - $190k / year
đź’° $625k Series B - WellRight on 2014-10
⏰ Full Time
đźź Senior
đź‘” Director
🦅 H1B Visa Sponsor
đź•’ Yesterday
Associate Director leading biostatistics for Cytel’s sponsor-dedicated pharmaceutical clinical trials. Guiding Phase 3 statistical activities, regulatory submissions, and advanced analytical methods.
đź•’ Yesterday
Lead GPS Group Peer Support training quality, fidelity, and trainer development. Build scalable systems and capacity for consistent national growth.
đź•’ Yesterday
Senior Director leading Fluxx’s Professional Services organization for its collaborative grantmaking platform. Driving profitable SaaS implementations, partner delivery, operational scale, and customer outcomes.
🇺🇸 United States – Remote
đź’µ $165k - $200k / year
đź’° $29.2M Venture Round on 2021-04
⏰ Full Time
đźź Senior
đź‘” Director