
201 - 500 employees
đź’Š Pharmaceuticals
🏥 Healthcare
đź’Ľ 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.
🔥 18 minutes ago
🗣️🇫🇷 French Required
Where this job comes from
Posted on Innovaderm Research Inc.'s careers page, not through a job board
First seen by Remote Rocketship 18 minutes ago

201 - 500 employees
đź’Š Pharmaceuticals
🏥 Healthcare
đź’Ľ 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.
• Manage and oversee clinical investigative sites and clinical monitoring deliverables for clinical trials • Ensure monitoring activities meet sponsor expectations, timelines, SOPs, regulations, GCP, and study-specific requirements • Identify quality issues and trends related to site performance and monitoring activities • Summarize findings and establish corrective action plans • Serve as point of contact for CRAs and Lead CRAs on assigned projects • Mentor and oversee CRAs and Lead CRAs • Review site visit reports and track metrics for compliance • Contribute to Clinical Monitoring Plan development • Prepare and conduct project-specific CRA training • Develop annotated site visit reports and monitoring tools, including source data verification worksheets • Conduct quality control and co-monitoring visits with CRAs • Coordinate and lead CRA meetings • Support business development activities, including client meetings, proposal defense meetings, RFPs, and RFIs
• B.Sc. in a field relevant to clinical research, nursing degree and/or equivalent experience • At least 8 years of clinical research experience, including prior monitoring experience • At least 2 years of experience as a Lead CRA or Clinical Team Leader in the biotechnology, pharmaceutical, and/or CRO industry • Strong knowledge of ICH/GCP standards and applicable regulatory requirements • Excellent mastery of Microsoft Office suite (Word, Excel, PowerPoint) • Ability to work in a fast-paced evolving environment and establish good relationships with colleagues, sites, and sponsors • Excellent leadership, organizational, time management, and multitasking skills • Excellent judgment and problem-solving skills • Occasional travel up to 10% of the time, including some travel outside Canada when possible • Fluent in English, with excellent oral and written skills • CRO and dermatology experience is an asset • Must be legally authorized to work in Canada
• Flexible work schedule • Home-based position • RRSP • Ongoing learning and development • Medical, dental, and vision insurance • Vacation days • Personal days • Virtual medical clinic • Public transit discounts • Social activities • Hybrid work option • Advancement opportunities • Permanent full-time position
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