
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 global pharmaceutical company that researches, develops, manufactures, and distributes prescription medicines and provides patient support services. The company focuses on life-changing medicines across conditions such as diabetes, cancer, Alzheimer’s disease, autoimmune disorders, dermatology, migraine, obesity, and sleep apnea; it runs clinical trials, offers LillyDirect pharmacy services, and emphasizes manufacturing quality, medication safety, and research into genetic medicines. Eli Lilly also provides patient resources, condition education, and access programs to help people find care and participate in trials.
🔥 4 hours ago
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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 global pharmaceutical company that researches, develops, manufactures, and distributes prescription medicines and provides patient support services. The company focuses on life-changing medicines across conditions such as diabetes, cancer, Alzheimer’s disease, autoimmune disorders, dermatology, migraine, obesity, and sleep apnea; it runs clinical trials, offers LillyDirect pharmacy services, and emphasizes manufacturing quality, medication safety, and research into genetic medicines. Eli Lilly also provides patient resources, condition education, and access programs to help people find care and participate in trials.
• Serve as a field-based scientific expert engaging healthcare professionals and supporting clinical development • Maintain therapeutic-area expertise and scientific knowledge aligned with Medical Affairs objectives • Engage in compliant, non-promotional scientific exchange with KOLs, investigators, and other healthcare professionals • Provide accurate and balanced medical information to external stakeholders • Deliver company-approved medical and scientific presentations to formulary committees and healthcare professionals • Support speaker training, advisory boards, and sales training as appropriate • Document field-based activities accurately, timely, and compliantly • Collaborate with Clinical Operations to identify and evaluate clinical trial sites and investigators • Provide scientific education and protocol-specific training during site initiation visits • Maintain engagement with trial sites and investigators to support trial execution, answer protocol inquiries, and facilitate high-quality data generation • Attend scientific and medical congresses and provide real-time insights and post-conference reports • Support congress activities through pre-conference planning, booth coverage, symposia participation, and KOL engagement • Contribute to scientific slide decks, FAQs, and educational materials • Write and edit Medical Information response letters • Ensure scientific materials are medically accurate, evidence-based, and compliant with regulatory standards • Collaborate with Medical Affairs and Legal teams on scientific content • Lead MSL strategic initiatives and projects • Develop scientific training plans for the MSL team • Mentor MSL peers
• Advanced degree (PhD, PharmD, MD) in life sciences or a related field from an accredited college or university • Minimum of 2 years of experience in a Medical Affairs or MSL role within the pharmaceutical or biotech industry • Excellent understanding of sleep medicine and associated therapeutic areas strongly preferred • Exceptional verbal and written communication skills; ability to tailor scientific messages to diverse audiences and interpret and communicate complex scientific data • Proven ability to build and maintain strong relationships with KOLs, investigators, and internal stakeholders • Strong understanding of clinical trial design, regulatory requirements, and therapeutic area landscape • Skilled in developing and delivering scientific presentations in various settings • Strong understanding of industry regulations and guidelines governing medical interactions • Ability to align field activities with broader medical and corporate strategies • Must have a valid driver’s license with a driving record that meets company requirements • Willing and able to travel frequently throughout the Southeast region, including Alabama, Arkansas, Florida, Georgia, Louisiana, Mississippi, South Carolina, and Tennessee • Must reside in the Atlanta metropolitan area or a major Florida metropolitan area with access to a major commercial airport • Remote role based in the United States with up to 60–70% travel and occasional weekends
• Company bonus depending on company and individual performance • Company-sponsored 401(k) • Pension • Vacation benefits • Medical, dental, vision, and prescription drug benefits • Flexible benefits, including healthcare and dependent day care flexible spending accounts • Life insurance and death benefits • Certain time off and leave of absence benefits • Well-being benefits, including employee assistance program, fitness benefits, and employee clubs and activities
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