
201 - 500 employés
💊 Pharmaceutique
🏥 Santé
💼 Conseil
Pharmaceuticals • Healthcare • Consulting
En tant qu'organisme de recherche sous contrat (CRO) spécialisé en dermatologie, nous offrons des conseils scientifiques, des résultats précis et la satisfaction du client. Notre offre de services unique combine des services de recherche sous contrat spécialisés, la connaissance des sites dermatologiques en Amérique du Nord et en Europe et les capacités étendues d'un grand site de recherche clinique.
🕒 il y a 25 jours
🗣️🇺🇸🇬🇧 Anglais requis
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201 - 500 employés
💊 Pharmaceutique
🏥 Santé
💼 Conseil
Pharmaceuticals • Healthcare • Consulting
En tant qu'organisme de recherche sous contrat (CRO) spécialisé en dermatologie, nous offrons des conseils scientifiques, des résultats précis et la satisfaction du client. Notre offre de services unique combine des services de recherche sous contrat spécialisés, la connaissance des sites dermatologiques en Amérique du Nord et en Europe et les capacités étendues d'un grand site de recherche clinique.
• Oversee a portfolio or program of clinical projects and the Project Managers assigned to operationalize awarded studies • Ensure studies reflect therapeutic-area and client-specific requirements • Represent the company to customers and maintain satisfaction levels • Communicate program deliverables effectively • Ensure studies progress according to quality standards, SOPs, GCPs, regulatory requirements, and ICH guidelines • Oversee executed contracts and financial aspects, including study budgets and expenses • Maintain and evaluate project progress using timelines and tracking/analysis tools • Maintain in-depth therapeutic and client-specific knowledge for assigned portfolios • Apply study-specific learning across assigned studies and clients • Lead contingency planning and risk-mitigation strategies • Lead operational input to proposal development and pricing, including operations strategy • Drive performance improvement, operational efficiencies, and innovative strategies • Provide line-management oversight and contribute to Project Management leadership as an operational and therapeutic-area expert
• Bachelor of Science in a relevant discipline • At least 15 years of industry experience • Minimum of 5 years at a CRO • At least 10 years of clinical project management experience, including management of all project phases from start-up to closure, all functional services, and vendor management • Experience in dermatology or rheumatology trials is required • Experience leading concurrent multicentered, multinational Phase III clinical trials, including project budget financial tracking and forecasting • Experience with mid-size and large studies (>10–15 countries) in multiple regions (NA, SA, APAC, MENA, Europe) is desirable • Substantial experience in project supervision, mentoring, and coaching of project managers • Substantial experience with business development tasks, including proposal development, client presentations, and bid defense meetings • Good knowledge of Good Clinical Practices and applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines • Applicants must be legally authorized to work in Germany
• Stimulating work environment • Attractive advancement opportunities • Regular travel, including potential overnight and international travel as part of the role • Accommodations throughout the recruitment and selection process for applicants with disabilities, upon request
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