Associate Centralized Monitoring Lead, Egypt
Associate Centralized Monitoring Lead
Egypt
Homebased
We are seeking a proactive and detail-oriented Associate Centralized Monitoring Lead 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 CMS Leads and project teams in executing centralized monitoring strategies aligned with study protocols, SOPs, and regulatory requirements.
Review site visit reports, identify risks, and ensure consistent quality standards across studies.
Analyze study and site metrics, trends, and triggers to detect risks and drive timely corrective actions.
Contribute to the development of monitoring plans, risk mitigation strategies, and analytics solutions.
Collaborate with cross-functional teams to ensure subject safety, data integrity, and regulatory compliance (ICH-GCP).
Support study operations including investigator payments, resource coordination, and documentation management.
Perform subject-level data reviews and ensure accuracy and quality of clinical data.
Assist in mentoring junior team members and driving continuous process improvements.
Requirements:
B Sc Degree in Life Sciences
Minimum 3 years’ 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 and data review 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.
Apply To This Job
Egypt
Homebased
We are seeking a proactive and detail-oriented Associate Centralized Monitoring Lead 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 CMS Leads and project teams in executing centralized monitoring strategies aligned with study protocols, SOPs, and regulatory requirements.
Review site visit reports, identify risks, and ensure consistent quality standards across studies.
Analyze study and site metrics, trends, and triggers to detect risks and drive timely corrective actions.
Contribute to the development of monitoring plans, risk mitigation strategies, and analytics solutions.
Collaborate with cross-functional teams to ensure subject safety, data integrity, and regulatory compliance (ICH-GCP).
Support study operations including investigator payments, resource coordination, and documentation management.
Perform subject-level data reviews and ensure accuracy and quality of clinical data.
Assist in mentoring junior team members and driving continuous process improvements.
Requirements:
B Sc Degree in Life Sciences
Minimum 3 years’ 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 and data review 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.
Apply To This Job