Become a Senior Clinical Associate at IQVIA in Montréal, contributing to the oversight of clinical trials and ensuring compliance with regulations. Bilingualism in French and English is essential.
The ideal candidate has a strong background in site management and at least three years of monitoring experience. Your responsibilities will include conducting comprehensive visits, guiding protocol training at sites, and actively managing recruitment and quality assessment efforts. This role plays a critical part in the success of our clinical studies.
Key Responsibilities:
• Lead site monitoring visits to ensure compliance
• Optimize subject recruitment and management plans
• Maintain site communication and training documentation
• Assess site practices for regulatory quality adherence
• Manage timelines and financial aspects of site agreements
Requirements:
• Bachelor’s degree in a relevant scientific field
• Three years’ experience in clinical site monitoring...