
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.
🔥 12 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 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 clinical scientist lead on one or more early-stage Phase 1/2 clinical trials for Orexin-targeted programs • Contribute to clinical development plan strategy, study design, dose-escalation/titration strategy, and data interpretation • Lead development, authorship, and review of clinical and cross-functional documents • Serve as study medical/scientific lead from study start-up through clinical study report completion • Drive dose-escalation and study conduct discussions through review of safety, PK/PD, and biomarker data • Provide scientific leadership in data review meetings, safety review committees, governance forums, and cross-functional discussions • Partner with Clinical Operations, Translational Science, Regulatory Affairs, Biostatistics, and Safety/Pharmacovigilance • Drive alignment and execution across functions for timely study delivery • Integrate biomarker and mechanistic hypotheses into clinical studies and development strategy • Identify and address scientific, operational, and strategic risks and gaps • Review and interpret clinical safety, efficacy, PK/PD, and exploratory biomarker data • Develop scientific insights and recommendations for clinical development decisions • Contribute to regulatory submissions, health authority responses, governance materials, and external scientific communications • Support abstracts, posters, manuscripts, and scientific meeting presentations • Lead interactions with investigators, CROs, vendors, external experts, key opinion leaders, and scientific advisory boards • Lead or support investigator meetings and scientific training sessions • Ensure organization and proactive management of study deliverables and workstreams • Mentor junior clinical scientists, depending on level
• Advanced scientific/clinical degree (PhD or PharmD) • 8–10 years of experience in clinical research or clinical development within the biotechnology or pharmaceutical industry • Strong scientific foundation in neuroscience/neurology required • Experience in neurodegeneration and/or neuropsychiatric indications strongly preferred • Deep understanding of clinical trial design, clinical data analysis, and drug development principles • Direct experience leading or supporting early-phase (Phase 1/2) clinical trials • Ability to independently lead complex scientific workstreams and influence cross-functional teams in a fast-paced biotech environment • Experience leading the development and authorship of clinical and regulatory documents, including protocols, IBs, CSRs, and briefing documents • Familiarity with Orexin biology or related sleep/wake and neurocircuitry mechanisms • Strong analytical and scientific interpretation skills • Excellent written and verbal communication skills • Ability to communicate complex scientific concepts to diverse audiences
• Company bonus depending partly on company and individual performance • Company-sponsored 401(k) • Pension • Vacation benefits • Medical benefits • Dental benefits • Vision benefits • Prescription drug benefits • Healthcare and/or dependent day care flexible spending accounts • Life insurance and death benefits • Time off and leave of absence benefits • Employee assistance program • Fitness benefits • Employee clubs and activities • Remote work with occasional travel
Apply Now🕒 2 days ago
Senior clinical scientist leading Phase 1/2 Orexin trials for Centessa Pharmaceuticals, developing medicines for narcolepsy and neurological disorders. Driving study strategy, clinical data interpretation, and regulatory documents.
🇺🇸 United States – Remote
💵 $168k - $283.8k / year
💰 $6.5M Post-IPO Debt - Eli Lilly on 2024-02
⏰ Full Time
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Clinical science advisor leading Phase 2–3 Orexin trials at Lilly/Centessa. Driving study execution, data interpretation, and clinical development for sleep-wake medicines.
🇺🇸 United States – Remote
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💰 $6.5M Post-IPO Debt - Eli Lilly on 2024-02
⏰ Full Time
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