
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.
đź•’ July 11
🗣️🇫🇷 French Required
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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.
• Responsible for the operational management and oversight of clinical investigative sites • Ensures that clinical monitoring activities are performed correctly and timely • Identifies quality issues and trends related to site performance • Serves as a point of contact for CRAs and Lead CRAs for assigned projects • Provides mentoring and oversight of CRAs and Lead CRAs • Prepares and conducts project-specific training for the CRAs • Develops annotated site visit reports and monitoring tools • Coordinates and leads CRA meetings
• 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 acting in a Lead CRA or Clinical Team Leader role in the biotechnology, pharmaceutical, and/or contract research organization (CRO) industry • Strong knowledge of ICH/GCP standards and applicable regulatory requirements • Excellent mastery of Microsoft Office suite (Word, Excel, Power Point) • Ability to work in a fast-paced evolving environment and establish good relationships with colleagues, sites and sponsors • Excellent leadership, organizational, time management and multi-tasking skills • Excellent judgement and problem-solving skills • Occasional travel (up to 10% of the time) • Fluent in English (excellent oral and written), French is an asset • Experience in a CRO and in dermatology an asset.
• Flexible work schedule • Complete benefits (medical, dental, vision, vacation, personal days, virtual medical clinic, social activities) • Ongoing learning and development
Apply Nowđź•’ July 9
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🗣️🇫🇷 French Required
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