Associate Centralized Monitor

Responsibilities

• Provide study-level administrative support to the clinical study management team, 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.
• 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 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 Good Clinical Practice (GCP) and relevant local regulatory requirements.
• Proficiency in clinical systems such as EDC, IXRS, and CTMS.
• Fluency in English, Czech, and Slovak.
• Advanced proficiency in Microsoft Office (Word, Excel, and PowerPoint).
• Strong analytical, 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.