Job Overview
Location
6 Locations
Job Type
Full-time
Category
HR & Recruiting
Date Posted
April 12, 2026
Full Job Description
đź“‹ Description
- • Lead the Centralized Monitoring team in LATAM to ensure clinical trial deliverables meet sponsor expectations for speed, quality, and cost while adhering to IQVIA SOPs and global regulatory standards.
- • Partner with project and clinical leads to oversee clinical deliverables, manage unblinded clinical lead responsibilities including IP management, and step in as Clinical Lead when needed during study execution or closeout.
- • Manage project resources including CRAs, Central Monitors, Clinical Trial Assistants, and Centralized Monitoring Assistants to ensure optimal team performance and workload distribution.
- • Monitor and analyze study/site metrics, develop analytics strategies, and apply advanced analytics to identify trends, triage alerts, and support continuous process improvement.
- • Contribute to monitoring strategy development, attend study team and client meetings, and provide inputs for issue escalation, workload projections, and quality integrity assessments.
- • Ensure complete and accurate documentation of study tools and templates, maintain audit readiness including eTMF oversight, and mentor junior staff to build team capability.
- • Operate across multiple global projects with competing priorities, requiring strong organizational, decision-making, and communication skills in a remote LATAM-based role.
🎯 Requirements
- • Bachelor’s degree in life sciences or a related field.
- • 3+ years of relevant clinical monitoring experience as a remote or on-site CRA with advanced knowledge of ICH GCP and applicable local regulations.
- • 2+ years in a lead role demonstrating leadership, mentoring, and team management capabilities.
- • Advanced command of English (written and verbal) is mandatory.
- • Strong organizational, problem-solving, decision-making, motivational, influencing, negotiating, and coaching skills.
- • Ability to manage multiple global projects and competing priorities effectively.
🏖️ Benefits
- • Opportunity to lead a centralized monitoring team in a global clinical research organization impacting patient health outcomes worldwide.
- • Remote work flexibility based in LATAM with collaboration across international project teams.
- • Professional growth through mentoring junior staff, leading complex studies, and developing advanced analytics capabilities.
- • Exposure to global clinical trial operations, regulatory standards, and IQVIA’s end-to-end healthcare intelligence solutions.
- • Role combines leadership, analytical, and strategic contributions in a mission-driven environment focused on accelerating medical innovation.
- • Access to IQVIA’s resources, training, and commitment to integrity and professional development in clinical research.
Skills & Technologies
About IQVIA Holdings Inc.
IQVIA Holdings Inc. provides advanced analytics, technology solutions, and clinical research services to the life-sciences industry. Formed through the 2016 merger of Quintiles and IMS Health, the company integrates healthcare data, analytics, and domain expertise to help biopharmaceutical and medical-device clients optimize drug development, commercialization, and real-world evidence generation. Its offerings span clinical trial design and execution, real-world insights, commercial strategy, and technology platforms that connect stakeholders across the healthcare ecosystem. Headquartered in Durham, North Carolina, IQVIA operates in more than 100 countries, supporting the development and delivery of therapies to improve patient outcomes worldwide.
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