Associate Centralized Monitor

Responsibilities

• Provide study-level administrative support to clinical study management teams, including running system reports and maintaining study trackers.
• Perform centralized monitoring activities on assigned sites to evaluate quality and integrity according to protocols and SOPs.
• Conduct Subject Level Data Review to ensure accuracy regarding inclusion/exclusion criteria, adverse events, and lab results.
• Manage operational insights for assigned sites, including trend analysis of clinical aspects and monitoring compliance with clinical operation plans.
• Facilitate early identification of site-level risks and recommend timely corrective actions.
• Interact with sites and CRAs to follow up on missing data, pending queries, and SDV backlogs.
• Assist in the preparation of i-site packs and maintain internal systems, databases, and project plans.

Requirements

• Graduate or Post Graduate degree in Life Sciences or a related field.
• 2 to 5 years of professional work experience, including at least 1 year of relevant experience in clinical research.
• Strong knowledge of ICH-GCP and applicable local regulatory requirements.
• Proficiency in clinical systems such as EDC, IXRS, and CTMS.
• Experience managing global phase trials and reviewing clinical trial data.
• Excellent written and verbal English communication skills.
• Proficiency in Microsoft Office applications (Word, Excel, PowerPoint).
• Strong attention to detail, problem-solving, and time management skills.

About the Company

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.