
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.
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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.
• Participate in development, conduct, and reporting of global clinical trials supporting product registration and commercialization • Implement global clinical trials and monitor patient safety and adverse-event follow-up • Review protocols, study reports, publications, labels, pricing, reimbursement, access documents, grants, and contracts • Serve as a scientific resource for study teams, departments, clinical operations personnel, investigators, and ethics boards • Collaborate on clinical strategy, lifecycle plans, development plans, and study protocol design • Design, conduct, and report local clinical trials and support study start-up, investigator training, and site activities • Review investigator-initiated trial proposals and publications • Address scientific information needs of healthcare professionals, investigators, patients, payers, and providers • Support symposia, advisory boards, congresses, medical information responses, data analyses, slide sets, abstracts, posters, and manuscripts • Establish relationships with external experts, thought leaders, professional societies, and the medical community • Provide medical expertise for regulatory reports, label changes, advisory committees, risk management, and registration efforts • Contribute to medical strategies, brand commercialization, payer partnership programs, product value defense, and strategic brand planning • Support promotional material development and define the patient journey and moments of truth • Evaluate medical literature, competitive products, clinical practice trends, and access developments • Provide scientific training and protocol expertise to clinical study teams • Support development budgets, professional development, recruitment, diversity, retention, committees, Six Sigma initiatives, and task forces • Collaborate with alliance, business, and vendor partners and model Lilly leadership behaviors
• Medical Doctor required • Board eligible or certified in an appropriate specialty/subspecialty, or comparable post-medical-school clinical training relevant to the hiring country • US-trained physicians must have achieved board eligibility or certification • Non-US-trained physicians must have completed education and training at a medical school meeting LCME requirements • Minimum 3 years of industry experience in oncology or malignant hematology preferred • Demonstrated experience and knowledge of clinical research and the drug development process • Strong communication, interpersonal, organizational, teamwork, and negotiation skills • Compliance with applicable local and international regulations, laws, guidance, Good Clinical Practices, company standards, policies, procedures, and integrity agreements • Maintain required qualifications and training, including a current curriculum training map
• Company bonus depending in part on company and individual performance • 401(k) participation • Pension • Vacation benefits • Medical benefits • Dental benefits • Vision benefits • 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 • Employee resource groups open to all employees
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