**Job Overview** ---------------- In line with the process of designing and launching global clinical research studies, conduct independent quality control (QC) reviews and ensure adherence to study set-up processes and procedures during start-up and amendment phases. Responsibilities include reviewing source documentation and database configuration against sponsor protocols, providing guidance on project design and organization, and developing and maintaining best practices within the organization. **Essential Functions** ----------------------- * Perform QC of project databases and requisition forms against sponsor protocols and specific requirements. * Collaborate cross-functionally to ensure QC reviews align with current processes and quality standards. * Work with Set-up Managers, Project Managers, and Set-up Coordinators to resolve issues or findings identified during QC reviews. * Oversee and maintain QC timelines to meet client needs. * Analyze and identify quality trends, recommending training and process improvements. * Partner with QC counterparts to ensure global consistency in study set-up processes. * Participate in external and internal audits as required. * Ensure all work complies with ICH E6 Guideline for Good Clinical Practice. **Qualifications** ------------------ * Bachelor’s degree in a science-related field required. * Minimum of 2 years of experience in the clinical or research industry, including at least 1 year in study set-up and/or project management. Equivalent combinations of education, training, and experience may be considered. * Strong interpersonal skills for interaction with senior internal stakeholders and, occasionally, senior sponsor representatives. * Proven ability to meet deadlines with high attention to detail, demonstrated in roles such as Set-up Manager, Senior Set-up Specialist, Project Manager, or equivalent. * Proficiency in Microsoft Office, Q² Solutions systems, and ELVIS. * Solid understanding of medical and clinical research terminology. * Ability to thrive in a fast-paced, deadline-driven environment. * Knowledge of set-up management and/or project management processes and terminology is an asset. * Excellent organizational and operational skills. * Strong written and verbal communication skills, with good command of English. * Ability to establish and maintain effective working relationships with colleagues, managers, and clients. You will be required to work directly with IQVIA departments, teams, support functions and stakeholders located across Canada and around the world therefore, a functional knowledge of English, both written and spoken, is necessary to perform the duties of this position. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com