
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.
🕒 September 4
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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.
• Serve as the main point of contact for site selection activities, including site identification and feasibility • Develop and maintain relationships with key clinical research sites • Identify investigators and research sites through literature and online searches • Collect information to define ideal investigators for studies • Identify and recommend potential investigators and sites • Develop interest survey assessments • Create and coordinate study-specific feasibility questionnaires • Review feasibility questionnaires and recommend sites for qualification visits • Coordinate CRA resource allocation for site qualification visits • Review site qualification visit summaries • Recommend sites for study participation in consultation with sponsors and project teams • Track site selection activities in the Clinical Trial Management System (CTMS) • Attend internal and external project team meetings as needed • Identify site performance quality issues through project meetings, escalated communications, and quality assurance audit findings • Participate in departmental projects related to site selection, contracting, and site intelligence • Support the Manager, Site Selection in understanding project goals, scope, and requirements and delivering high-quality results
• Bachelor’s degree in science or relevant field of study • Excellent oral and written skills in English; French is an asset • Minimum of 3 years of experience in clinical research in the biotechnology, pharmaceutical, or CRO industry • Significant and relevant experience in site selection, study start-up activities, site budget/contract negotiation, and/or working closely with sites or in a site environment • Excellent knowledge of Microsoft Office suite (Word, Excel, PowerPoint) • Experience in dermatological clinical research is an asset • Good knowledge of good clinical practices and applicable Health Canada and FDA regulations/guidelines • Ability to work in a team environment and establish good relationships with colleagues, sponsors, and sites • Organized, able to juggle competing priorities, and work in a fast-paced, evolving environment • Flexibility, positive attitude, superior attention to detail, and critical thinking skills • Quick learner, good adaptability, and versatility • Must be legally able to work in Poland
• Permanent full-time position • Flexible schedule • Vacation • Home-based position • Ongoing learning and development • Attractive advancement opportunities • Accommodation throughout the recruitment and selection process for applicants with disabilities, upon request
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