
51 - 200 employees
Founded 2020
đź’Ľ Consulting
🏥 Healthcare
📦 Logistics
đź’° Pre Seed Round on 2022-03
Consulting • Healthcare • Logistics
Lifelancer is an AI-powered talent hiring platform that connects employers with skilled professionals in the Life Sciences, Pharmaceutical, and IT sectors. It enables individuals to create profiles showcasing their skills, get matched with high-paying international jobs or projects, and facilitates hiring and payroll for employers in multiple countries. The platform aims to streamline the hiring process with efficient AI sourcing and compliance support.
đź•’ Yesterday
🇺🇸 United States – Remote
đź’µ $153k - $268.4k / year
⏰ Full Time
đźź Senior
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51 - 200 employees
Founded 2020
đź’Ľ Consulting
🏥 Healthcare
📦 Logistics
đź’° Pre Seed Round on 2022-03
Consulting • Healthcare • Logistics
Lifelancer is an AI-powered talent hiring platform that connects employers with skilled professionals in the Life Sciences, Pharmaceutical, and IT sectors. It enables individuals to create profiles showcasing their skills, get matched with high-paying international jobs or projects, and facilitates hiring and payroll for employers in multiple countries. The platform aims to streamline the hiring process with efficient AI sourcing and compliance support.
• Serve as clinical scientist on one or more late-stage (Phase 2-3) global clinical trials for Orexin-targeted sleep/wake programs • Support creation and review of clinical slides for investigator meetings, SIVs, IDMCs, advisory boards, and other meetings • Author or review protocols, Clinical Study Reports, Investigator Brochures, Development Safety Update Reports, and other study documents • Serve as study scientific expert from startup through Clinical Study Report completion • Support CRF design, enrollment monitoring, and patient profile review • Liaise with Clinical Operations on site selection, startup, study management, and closeout • Serve as primary contact for clinical inquiries from sites, CROs, site monitors, and health authorities • Integrate clinical and regulatory strategy into global product development strategy • Review clinical data for safety, data integrity, protocol compliance, and study performance • Lead cross-functional collaboration with Clinical Operations, Regulatory Affairs, Biostatistics, and Safety/Pharmacovigilance • Identify and address scientific, operational, and strategic risks and gaps • Develop scientific insights and recommendations for clinical development decisions • Partner with biostatistics on SAP development and review and interpretation of final clinical study TLFs • Support abstracts, posters, manuscripts, and scientific presentations • Provide scientific leadership with investigators, CROs, vendors, external experts, key opinion leaders, and scientific advisory boards • Manage deliverables across assigned studies and workstreams
• Advanced scientific/clinical degree (PhD or PharmD) with 2+ years drug development experience in the biotech/pharma industry, OR BS/MS in a scientific discipline with 8+ years drug development experience in the biotech/pharma industry • Strong scientific foundation in neuroscience/neurology • Understanding of clinical trial design, clinical data analysis, and drug development principles • Demonstrated accountability for delivery on clinical studies • Proven experience developing and authoring clinical and regulatory documents, including protocols, IBs, CSRs, and briefing documents • Familiarity with Orexin biology or related sleep/wake and neurocircuitry mechanisms preferred • Detail oriented with exceptional organizational skills • Effective verbal and written communication skills • Ability to identify issues, analyze situations, and provide effective solutions • Ability to partner with cross-functional teams in a fast-paced biotech environment • Role based in the United States • Occasional travel
• Company bonus based partly on company and individual performance • Company-sponsored 401(k) • Pension • Vacation benefits • Medical, dental, vision, and 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 Nowđź•’ 3 days ago
Senior Advisor leading delivery of Massachusetts’s statewide vaccine management and clinical case management system. Translating local health department needs into product requirements, workflows, and adoption strategies.
đź•’ October 10
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
đź’µ $153k - $268.4k / year
đź’° $6.5M Post-IPO Debt - Eli Lilly on 2024-02
⏰ Full Time
đźź Senior
đź•’ October 10
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
đź’µ $168k - $283.8k / year
đź’° $6.5M Post-IPO Debt - Eli Lilly on 2024-02
⏰ Full Time
đźź Senior
đź•’ October 9
Clinical science leader advancing Centessa’s Orexin medicines through Phase 1/2 trials. Guiding study design, data interpretation, regulatory documents, and cross-functional development strategy.
🇺🇸 United States – Remote
đź’µ $168k - $283.8k / year
đź’° $6.5M Post-IPO Debt - Eli Lilly on 2024-02
⏰ Full Time
đźź Senior
đź•’ October 9
Clinical scientist leading Phase 2-3 Orexin trials for Centessa, Lilly’s sleep-medicine subsidiary. Driving study strategy, execution, data review, and regulatory documentation.
🇺🇸 United States – Remote
đź’µ $153k - $268.4k / year
đź’° $6.5M Post-IPO Debt - Eli Lilly on 2024-02
⏰ Full Time
đźź Senior