
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.
🔥 3 hours ago
🏄 California, Idaho, +3 more states – Remote
💵 $156k - $250.8k / year
⏰ Full Time
🟠 Senior
👨⚕️ Medical Director
👻 Ghost score 0%
Improve your chances of getting an interview by checking your resume score before you apply.

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.
• Serve as a major Lilly representative for healthcare professionals, providing advanced disease-state and product information • Facilitate scientific exchange between Lilly and scientific and clinical experts • Connect scientific experts with Lilly resources such as Discovery Scientists, Outcomes Research, Clinical Development Consultants, and Clinical Research Physicians • Liaise between Lilly resources, Medical Affairs, Clinical Development, Brand teams, and external experts • Report clinical insights and unanswered customer questions to medical affairs, clinical development, and brand teams • Maintain technical expertise within a therapeutically aligned hematologic malignancies tumor team • Engage in continuous learning, attend scientific meetings, and conduct routine literature searches • Communicate relevant learning with peers • Support community and academic scientific experts with unsolicited requests for information on late- and early-phase hematologic malignancy agents • Develop and execute strategic territory plans, prioritize activities, and use territory analytics for customer identification and routing • Collaborate compliantly with Lilly field roles sharing customers • Synthesize and communicate actionable customer and clinical insights to internal medical and cross-functional teams • Cultivate internal networks, collaborate across functions, and contribute to team goals • Execute the role in compliance with internal and external requirements, procedures, and laws
• Advanced degree in health sciences (e.g., PharmD, MD, PhD in a medically related field) required • 2–3 years of relevant clinical or therapeutic area experience desired • Master's or bachelor's level degree in health sciences (e.g., BSN, RPh, PA, NP) considered if 5 or more years of clinical, research, or industry experience in the relevant therapeutic area is present • Valid US driver's license and acceptable driving record required • Authorized to work in the United States on a full-time basis; Lilly will not provide work authorization or visa sponsorship • Clinical oncology experience, including experience with physicians, nurses, nurse practitioners, or pharmacists working with patients in hospital or outpatient clinical settings • Ability to use field-based electronic or other communication tools • Ability to comprehend and communicate large amounts of scientific content clearly and concisely • Direct experience servicing customer needs for complex information • Experience working with demanding or difficult clients • Experience self-managing priorities and multitasking projects • Strong teamwork and interpersonal skills • Advanced presentation and computer skills, with expertise in literature identification and evaluation • Experience in professional networking with positive, mutually meaningful outcomes • Familiarity with the academic community and medical research and education processes highly valued • Effective verbal and written communication skills • Ability to travel overnight up to 60% and work 4–6 weekends per year
• Company bonus depending in part 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 • Certain time off and leave of absence benefits • Well-being benefits, including employee assistance program, fitness benefits, and employee clubs and activities
Apply Now🔥 4 hours ago
Market Physician Executive leading Monogram Health’s in-home, evidence-based chronic care for complex patients across Georgia. Directing clinical teams, population health strategies, and patient outcomes.
🕒 3 days ago
Associate Director guiding patient-centered clinical outcome assessment strategy for Otsuka clinical programs. Developing regulatory evidence and endpoint strategies across global cross-functional teams.
🕒 4 days ago
Senior Medical Director guiding clinical-trial medical strategy, monitoring, and client development at Fortrea, a global clinical research organization. Leading therapeutic expertise, safety oversight, and investigator collaboration.
🇺🇸 United States – Remote
💵 $173k - $320k / year
💰 Pre Seed Round on 2022-03
⏰ Full Time
🟠 Senior
👨⚕️ Medical Director
🕒 4 days ago
Senior Medical Director directing medical strategy, monitoring, and client support for Fortrea’s clinical trials. Leading therapeutic-area expertise, safety oversight, and investigator collaboration.
🕒 5 days ago
Associate Director managing global clinical supply planning, forecasting, vendors, and regulatory compliance for Liquidia’s pulmonary hypertension therapies. Ensuring uninterrupted trial material availability worldwide.