Medical Director, CMH – IBU Alliance Markets

🔥 0 minutes ago

🌐 United Kingdom, South Africa, +4 more countries – Remote

🇬🇧 United Kingdom – Remote 🇿🇦 South Africa – Remote 🇪🇬 Egypt – Remote 🇹🇭 Thailand – Remote 🇲🇾 Malaysia – Remote 🇸🇬 Singapore – Remote

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

👻 Ghost score 10%

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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

• Understand and anticipate scientific information needs of local and regional customers, including payers, patients, and health care providers • Lead data analyses and new clinical or health outcomes research efforts to address customer questions • Contribute to medical strategies supporting brand commercialization activities • Collaborate with global Medical Affairs, brand, patient outcomes/real-world evidence, clinical management, and cross-functional teams on local business plans • Comply with local laws, regulations, global policies, procedures, and compliance guidelines for data dissemination and interactions with external health care professionals • Address unsolicited scientific information requests from external health care professionals • Support preparation and review of medical letters and medical information materials • Establish and maintain collaborations with external scientific experts, thought leaders, and the broader medical community • Represent country or regional clinical needs in clinical strategy, 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 • Participate in development and review of local labeling and labeling modifications • Provide medical expertise to regulatory scientists and participate in advisory committees • Monitor clinical practice and access trends in relevant therapeutic areas • Evaluate medical literature, competitive product data, and scientific developments • Act as scientific consultant and protocol expert for clinical study teams and medical colleagues

🎯 Requirements

• Medical Doctor or Doctor of Osteopathy • Must be board eligible or certified in an appropriate specialty/subspecialty, or have completed comparable post-medical-school clinical training relevant to the country of hiring • Must have completed education and training at a medical school that meets the requirements of the Liaison Committee on Medical Education • Fluent in English, both verbal and written communication • Knowledge of the drug development process relevant to the country/region preferred • Strong communication, organizational, and negotiation skills • Demonstrated ability to influence others to create a positive working environment

🏖️ Benefits

• Disability accommodation support during the application process • Equal employment opportunity and non-discrimination commitment