
201 - 500 employees
💊 Pharmaceuticals
🏥 Healthcare
💼 Consulting
Pharmaceuticals • Healthcare • Consulting
Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.
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201 - 500 employees
💊 Pharmaceuticals
🏥 Healthcare
💼 Consulting
Pharmaceuticals • Healthcare • Consulting
Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.
• Oversee a portfolio or program of clinical studies and the Project Managers assigned to operationalize awarded studies • Ensure studies reflect therapeutic-area and client-specific requirements • Represent Indero to customers, maintain satisfaction levels, and communicate program deliverables • 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/or client-specific knowledge for the assigned portfolio • 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
• At least 15 years 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 with mid-size and large studies (>10–15 countries) in multiple regions (NA, SA, APAC, MENA, Europe) is desirable • Experience leading concurrent multicentered, multinational Phase III clinical trials, including project budget financial tracking and forecasting • Substantial experience in project supervision, mentoring, and coaching project managers • Substantial experience with business development tasks, including proposal development, client presentations, and bid defense meetings • Participation in mentoring and coaching of a representative number of project managers • Bachelor of Science in a relevant discipline • PMP or PRINCE2 Certification is an asset • Master's degree is an asset • Good knowledge of Good Clinical Practices and applicable Health Canada and FDA regulations/guidelines • Must be legally able to work in Europe
• Flexible work schedule • Home-based position • Ongoing learning and development • Attractive advancement opportunities • Equitable treatment and equal opportunity • Accommodations throughout the recruitment and selection process for applicants with disabilities, upon request
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