
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.
🔥 2 minutes 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 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.
• Drive execution of Lilly clinical trials through investigator engagement and site performance management • Manage investigator engagement from identification and qualification through enrollment, database lock support, and study closeout • Ensure investigators understand protocol intent, scientific rationale, and patient eligibility requirements • Build and sustain strategic relationships with investigators across trials and therapeutic areas • Co-create tailored recruitment strategies and identify opportunities to reach new patients and accelerate enrollment • Capture and elevate site insights to optimize feasibility, protocol design, and study conduct • Lead site-level strategy and risk planning for enrollment and data delivery • Use performance metrics to anticipate issues, intervene, and maintain clinical milestone momentum • Drive continuous inspection readiness across sites • Collaborate with internal functions and vendors to resolve operational barriers and ensure quality delivery • Influence country/site selection and protocol localization using local treatment paradigms and standards of care • Provide oversight and quality assurance for vendor monitoring and proactively escalate risks • Where applicable, manage Post-Marketing Safety Studies end to end in compliance with local regulations • Cultivate a strategically aligned portfolio of high-impact investigators • Serve as a scientific liaison among field teams, vendors, investigators, regulatory agencies, ethics committees, and national research organizations where applicable • Contribute to regional initiatives and enterprise-wide clinical development success
• Bachelor’s degree or equivalent; scientific, clinical, or health-related fields strongly preferred • Minimum 5 years of experience in clinical research or the pharmaceutical industry • Experience directly interacting with or working with healthcare professionals and clinical sites • Must reside in California to support the West Coast Region • Advanced degree in a scientific or clinical field preferred, including PharmD, PhD, MD, or MSc • Experience in immunology therapeutic areas, including dermatology, allergy, or respiratory • Excellent understanding of GCP, clinical development and operations, and the trial lifecycle • Understanding of therapeutic landscapes and standards of care • Ability to build credibility and influence healthcare professional communities through scientific expertise and relationships • Data-driven decision-making and ability to interpret operational and performance metrics • Excellent communication, negotiation, and organizational skills • Deep therapeutic-area knowledge and familiarity with local clinical research ecosystems • Experience influencing clinical site performance and driving enrollment success • Track record of delivering or exceeding performance targets in a collaborative matrix environment • Experience working with regulators or national bodies in support of clinical trial delivery • English fluency and proficiency in local language(s) as needed • Willingness to travel extensively (60-80%)
• 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 • Time off and leave of absence benefits • Well-being benefits, including employee assistance program, fitness benefits, and employee clubs and activities • Employee resource groups and support networks
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