
201 - 500 employés
Fondée en 2003
🏥 Santé
💼 Conseil
📣 Marketing
🔥 Financement dans la dernière année
💰 €500 000 000 Post-IPO Equity - Summit Therapeutics en 2025-10
Healthcare • Consulting • Marketing
Summit Therapeutics, Inc. est une entreprise biopharmaceutique spécialisée en oncologie, axée sur la découverte, le développement et la commercialisation de nouvelles thérapies médicales visant à améliorer la qualité et la durée de vie des patients avec des besoins médicaux non satisfaits. La société développe l'ivonescimab (SMT112), un nouvel anticorps bispécifique ciblant le PD-1 et le VEGF, à travers plusieurs essais cliniques de Phase 3 pour le cancer du poumon non à petites cellules et d'autres tumeurs solides sous licence d'Akeso. Summit met l'accent sur le développement clinique, les stratégies de dépôt réglementaire et la commercialisation potentielle dans ses territoires sous licence tout en promouvant des options de traitement adaptées aux patients et aux soignants.
🕒 il y a 10 jours
🇺🇸 États-Unis – Télétravail
💵 $169 000 - $198 000 / an
⏰ Temps Plein
🟠 Senior
👔 Directeur
👻 Score fantôme 1%
🗣️🇺🇸🇬🇧 Anglais requis
D'où vient cette offre
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Repérée par Remote Rocketship il y a 10 jours
Toujours ouverte sur le site de Summit Therapeutics, Inc.. Vérifiée il y a 1 heure.

201 - 500 employés
Fondée en 2003
🏥 Santé
💼 Conseil
📣 Marketing
🔥 Financement dans la dernière année
💰 €500 000 000 Post-IPO Equity - Summit Therapeutics en 2025-10
Healthcare • Consulting • Marketing
Summit Therapeutics, Inc. est une entreprise biopharmaceutique spécialisée en oncologie, axée sur la découverte, le développement et la commercialisation de nouvelles thérapies médicales visant à améliorer la qualité et la durée de vie des patients avec des besoins médicaux non satisfaits. La société développe l'ivonescimab (SMT112), un nouvel anticorps bispécifique ciblant le PD-1 et le VEGF, à travers plusieurs essais cliniques de Phase 3 pour le cancer du poumon non à petites cellules et d'autres tumeurs solides sous licence d'Akeso. Summit met l'accent sur le développement clinique, les stratégies de dépôt réglementaire et la commercialisation potentielle dans ses territoires sous licence tout en promouvant des options de traitement adaptées aux patients et aux soignants.
• Develop and execute site alliance strategies and maintain strategic relationships with clinical institutions, investigators, research staff, and site leadership • Lead start-up optimization with internal and external Study Start-Up teams through early engagement, MSAs, standardized budgets and contracts, and streamlined processes • Serve as the primary Clinical Operations interface and escalation point for site alliance matters • Partner with study teams, CROs, vendors, and functional leaders to resolve operational issues, reduce site burden, and improve external partner performance • Align site engagement activities with study and Summit priorities across Clinical Operations, Medical Affairs, Clinical Science, Regulatory, Quality, Data Management, Pharmacovigilance, and external partners • Identify, onboard, educate, and cultivate new sites for current and future portfolio needs • Develop and monitor KPIs, dashboards, and relationship health measures • Contribute site and network insights to portfolio planning, resource forecasting, and operational prioritization • Contribute to Clinical Operations strategy and transformation initiatives • Simplify clinical trial processes and improve site and patient experience • Advance process efficiencies, vendor optimization, and operational standardization initiatives • Develop recommendations and business cases to improve quality, timelines, and cost effectiveness • Champion collaboration, accountability, learning, and continuous improvement; may coach or mentor Clinical Operations colleagues • Perform other duties as assigned
• Bachelor’s degree or equivalent in life science, nursing, pharmacy, medical laboratory technology, or other health/medical-related area required; advanced degree preferred • 10+ years of direct or indirect clinical trial operations experience, including clinical trial execution, site management, site engagement, or sponsor oversight responsibilities • 3+ years of experience in a site-facing clinical trial role strongly preferred • Experience hiring, developing, mentoring, or actively managing team members directly or through a matrixed structure preferred • Experience building and managing strategic relationships with clinical trial sites, site networks, investigators, and external research partners • Strong working knowledge of ICH-GCP, health authority expectations, clinical trial conduct, sponsor oversight, and inspection readiness requirements • Ability to travel domestically and internationally, as required; anticipated travel up to 25–30% • Strong communication, negotiation, and relationship management skills • Broad expertise across clinical trial operations, including site start-up, enrollment, site and patient experience, sponsor oversight, and the drug development lifecycle • Ability to influence, build alignment, and support accountability across cross-functional, matrixed, and external stakeholder groups • Demonstrated ability to translate data, KPIs, and site insights into strategic recommendations and measurable operational improvements
• Potential bonus • Stock • Benefits • Other applicable variable compensation
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