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- ...Lead global site activation strategies across multiple regions to accelerate clinical trial enrollment. Manage site identification, regulatory submissions, contracting, and lifecycle operations while ensuring compliance with ICH-GCP standards and project timelines....
- ...IQVIA seeks an Associate Site Activation Manager to lead global clinical trial start-up and site activation activities across multiple regions. The role involves partnering with sponsors and investigative sites to accelerate patient enrollment, drive regulatory submissions...
- ...IQVIA seeks a Site Activation Coordinator to support feasibility assessments and site initiation activities for clinical research studies across North America. The role involves managing site documentation, tracking regulatory submissions, and serving as primary contact...
- ...IQVIA seeks a senior site activation specialist based in Argentina or Brazil to coordinate clinical trial site preparation activities across North American studies. The role involves managing documentation, regulatory compliance, and communication between investigative...
- ...IQVIA seeks a Site Activation Specialist for its North America team based in Argentina or Brazil. The role involves managing site feasibility, regulatory documentation, contracting, and performance tracking for clinical research studies, working closely with project teams...
- ...their maintenance phase. The position involves coordinating with cross-functional teams to ensure timely completion of regulatory activities, system management, and compliance tracking across assigned studies. Responsibilities Maintain and update internal systems,...
- ...and anything you and your team can build to drive real impact. AI-assisted engineering is an integral part of how we work. We actively use AI agents to accelerate software development, troubleshoot complex issues, and assist with deployments and operational workflows...
- ...Strategists. They are known for their reliability and attention to detail, resulting in high-quality work delivered on time. They are actively involved in supporting reporting, optimizations, and routine campaign management. They are a self-starter when it comes to their...
- ...between study teams and clinical program leadership. Responsibilities Lead cross-functional study teams and oversee outsourced activities to achieve milestones within budget and quality standards Develop and maintain study-level documents, plans, and quality/risk...
- ...Partner with operational and sponsor teams to strengthen quality performance and regulatory compliance Lead quality governance activities and facilitate quality decision-making across clinical programs Identify, assess, and mitigate quality risks throughout study...
- ...valuable deliverables.. - Maintain reliable systems by applying best practices for observability, quality, and incident response, and actively use AI tooling to detect, diagnose, and resolve issues faster.. - Support production releases, ensuring your team's systems are...