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.
Skills Required
- BSc degree in Life Sciences
- Minimum 1 year of 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 and cross-functional collaboration skills
- Ability to manage multiple priorities and deliver quality results within timelines
- Experience with clinical systems
IQVIA Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about IQVIA and has not been reviewed or approved by IQVIA.
-
Healthcare Strength — Healthcare coverage is positioned as comprehensive, spanning medical/dental/vision plus programs like telemedicine, EAP resources, and additional insurance options. Feedback suggests the health offering is a meaningful part of the overall rewards package, though details can vary by location and plan design.
-
Retirement Support — Retirement benefits include an employer match structure that supports employee contributions through a defined formula. This adds steady long-term value to total rewards beyond base salary.
-
Leave & Time Off Breadth — Time off offerings include vacation/paid time off, holidays, and flexibility themes, with some roles described as having discretionary or unlimited time-off models. This can make the package feel more attractive even when cash compensation is viewed as only mid-range.
IQVIA Insights
What We Do
IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 70,000 employees, IQVIA conducts operations in more than 100 countries. To learn more, visit www.iqvia.com.
