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The Associate Centralized Monitor supports clinical trial delivery by reviewing site data, performance metrics, and risks to ensure compliance and data integrity. They collaborate with project teams and sites to resolve queries and maintain essential study documentation.
Associate Centralized Monitor
Egypt
Homebased
We are seeking a proactive and detail-oriented Associate Centralized Monitor to support the successful delivery of clinical trials through high-quality centralized monitoring and cross-functional collaboration.
Summary:
Provides support to CMS Leads in delivering centralized monitoring activities in collaboration with project and clinical teams, ensuring project objectives are met with optimal quality, efficiency, and compliance. Focuses on identifying and addressing clinical risks through effective monitoring strategies and implementation. Ensures high-quality review of Site Visit Reports, maintaining consistent standards, safeguarding subject safety and data integrity, and escalating issues in line with SOPs, ICH-GCP, and regulatory requirements. Contributes to and reviews the Study Central Monitoring Plan.
Key Responsibilities:
Support centralized monitoring activities to ensure site quality, compliance, and data integrity.
Review clinical trial data, site performance metrics, trends, and risks; escalate issues and support corrective actions.
Collaborate with sites and CRAs to resolve data queries, protocol deviations, and study-related issues.
Prepare and maintain study reports, trackers, site packs, and monitoring documentation.
Perform subject-level data review and study-specific analytics.
Support study systems, access management activities, and process compliance.
Maintain effective communication with study teams and stakeholders.
Provide backup support to Centralized Monitors and assist with continuous process improvement initiatives.
Requirements:
B Sc Degree in Life Sciences
Minimum 1 year experience in clinical research or a related field.
Strong knowledge of ICH-GCP, clinical trial processes, and regulatory requirements.
Excellent analytical, organizational, and problem-solving skills.
Strong communication skills with the ability to collaborate across global teams.
Ability to manage multiple priorities and deliver high-quality results within timelines.
Experience with clinical systems is highly advantageous.
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
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
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