Director, Medical Affairs

🔥 0 minutes ago

🌐 Egypt, Ireland, +2 more countries – Remote

🇪🇬 Egypt – Remote 🇮🇪 Ireland – Remote 🇬🇧 United Kingdom – Remote 🇿🇦 South Africa – Remote

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

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Eli Lilly and Company

WebsiteLinkedInAll Job Openings

10,000+ employees

💊 Pharmaceuticals

🏥 Healthcare

🧬 Biotechnology

💰 $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.

📋 Description

• Provide expert scientific and clinical support to all aspects of the CMH regional business • Lead strategic planning for launch and commercialization activities within Medical Affairs Alliances • Work closely with Global and IBU CMH teams and lead the Alliances Lilly CMH expert community, including direct reports • Ensure alliances medical activities comply with local and international regulations, laws, guidance, GCPs, company standards, Lilly policies, quality standards, and Medical Research principles • Understand and anticipate scientific information needs of payers, patients, and healthcare providers • Lead data analyses and new clinical or health outcomes research efforts • Develop and implement medical strategies supporting brand commercialization • Educate the peer network and contribute to regional promotional-material development, review, and approval • Represent country or regional clinical needs in clinical strategies, development plans, and study protocol design • Review and approve local informed-consent documents and risk profiles • Collaborate on the design, conduct, and reporting of local clinical trials • Address unsolicited scientific information requests from external healthcare professionals • Support symposia, advisory boards, healthcare-professional meetings, medical letters, and medical-information materials • Establish relationships with external scientific experts, thought leaders, and the medical community • Participate in local labeling and labeling-modification development and review • Provide medical expertise to regulatory scientists and participate in advisory committees

🎯 Requirements

• Deep scientific expertise and knowledge of CMH and its treatment • Comfortable interpreting technical scientific/medical data and research and communicating with credibility, with good presentation skills • Understanding of the CMH customer and CMH business, with strong planning and execution skills • Evidence of good teamwork in a cross-functional environment and interpersonal skills • Strong communication, organizational, and negotiation skills • People management skills • Willingness to travel to customers, meetings, and congresses within the Alliances and internationally • Knowledge of and compliance with local laws and regulations, global policies and procedures, and compliance guidelines for data dissemination and interactions with external healthcare professionals

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