
51 - 200 employés
⚕️ Assurance santé
☁️ SaaS
💊 Pharmaceutique
💰 €9 000 000 Series B en 2022-01
Healthcare Insurance • SaaS • Pharmaceuticals
CRIO est une plateforme intuitive de logiciels eSource et d'essais cliniques qui capture les données guidées par le protocole directement au point d'interaction avec le patient pour réduire la charge des sites et améliorer la qualité des données. Conçu par des experts en recherche clinique, CRIO offre des modèles configurables, un accès en temps réel aux données pour une surveillance à distance, des outils intégrés de reporting et de requête, ainsi qu'un écosystème connecté incluant des modules eSource, EDC, eConsent, CTMS et eRéglementaire. Il sert les promoteurs, les CRO et les sites cliniques pour accélérer le démarrage des études, augmenter le recrutement et réduire les déviations du protocole.
🕒 il y a 8 jours
🇺🇸 États-Unis – Télétravail
💵 $85 000 - $98 000 / an
⏰ Temps Plein
🟡 Intermédiaire
🟠 Senior
👷♀️ Chef de Projet
🗣️🇺🇸🇬🇧 Anglais requis
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51 - 200 employés
⚕️ Assurance santé
☁️ SaaS
💊 Pharmaceutique
💰 €9 000 000 Series B en 2022-01
Healthcare Insurance • SaaS • Pharmaceuticals
CRIO est une plateforme intuitive de logiciels eSource et d'essais cliniques qui capture les données guidées par le protocole directement au point d'interaction avec le patient pour réduire la charge des sites et améliorer la qualité des données. Conçu par des experts en recherche clinique, CRIO offre des modèles configurables, un accès en temps réel aux données pour une surveillance à distance, des outils intégrés de reporting et de requête, ainsi qu'un écosystème connecté incluant des modules eSource, EDC, eConsent, CTMS et eRéglementaire. Il sert les promoteurs, les CRO et les sites cliniques pour accélérer le démarrage des études, augmenter le recrutement et réduire les déviations du protocole.
• Develop and Lead Clinical Trial Delivery Programs: Help to implement best practice work plans for sponsor and CRO-facing implementations, emphasizing clinical trial delivery and tech capability transfer. Support target service levels focused on quality, efficiency, and client satisfaction. Contribute to RFP responses and guide product roadmap decisions. Surface and expand on strategic vendor partnerships and identify essential integrations for a seamless end-to-end clinical trial workflow. • Help to continue to establish a Site Selection Program: Promote CRIO’s Site Directory as a site selection and performance evaluation tool. Support a data-driven service to assist sponsors in identifying top-performing CRIO sites. Define and monitor key performance metrics to measure site success. • Serve as a Clinical Project Manager: Support existing SPMs in day to day tasks and assist with larger project management as needed. Lead project execution by collaborating with clients to understand project needs, strategies, and deliverables. Guide clients through CRIO platform implementation, process changes, and operational enhancements. Address client concerns, manage escalations, and ensure high client satisfaction throughout the project lifecycle. • Drive Team Productivity and Efficiency: Contribute to project staffing, progress monitoring, and workload management to ensure timely and budget-conscious delivery. Collaborate with senior management to prioritize deliverables for multiple concurrent projects. Interface with internal teams and external vendors (IRT, eCOA, labs) to ensure seamless project execution. Assess CRIO’s service level offerings and propose enhancements for better efficiency and quality. • Support Sales and Marketing Efforts: Partner with sales and marketing to develop and deliver compelling capabilities presentations. Act as a CRIO representative at professional meetings, promoting CRIO’s vision and offerings. • Contribute to Organizational Development: Continuously explore ways to improve departmental processes and cross-departmental collaboration. Take on additional responsibilities as necessary to support organizational growth. • Maintain Industry Knowledge: Stay updated on clinical research trends, client needs, and regulatory developments. Participate in company-sponsored training to enhance technical and industry expertise.
• Bachelor’s degree in life sciences, pharmacy, or nursing; Master’s degree preferred. • 5+ years of clinical trial experience in a CRO or pharmaceutical research organization, with project management experience required. • Strong knowledge of GCP, ICH guidelines, and FDA regulations. • Experience with EDC, eSource, or DDC systems preferred. • Exceptional interpersonal, organizational, and leadership skills. • Strong written and verbal communication abilities. • Goal-oriented with a hands-on approach to problem-solving. • Proficient in Microsoft Office Suite and project management tools. • Google Suite knowledge and Looker tools experience.
• Work from anywhere • Unlimited PTO • 401k company match • Healthcare • Dental • Vision (Company Paid 100%) • Life insurance • Professional Development Reimbursement • Work From Home Expense Reimbursement
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