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IQVIA is seeking a Clinical Project Manager Sponsor-dedicated to manage local clinical trials in a hybrid capacity. This full-time role involves overseeing clinical trials from start-up to database lock and closeout activities, ensuring compliance with company SOPs, ICH-GCP guidelines, and regulatory requirements. The position includes collaboration with the clinical trial team to deliver high-quality data and meet recruitment targets while maintaining trial compliance. Candidates should have more than 2 years of clinical trial management experience and be fluent in both Arabic and English.
Key Responsibilities:
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Manage the operational oversight of clinical trials at the country level.
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Ensure the local trial team delivers quality data and trial documents compliant with protocols and regulatory requirements.
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Act as the primary contact for assigned trials at the country level.
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Ensure local/country team meets recruitment targets with high-quality data within the study budget.
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Contribute to site-level recruitment strategies and vendor management.
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Ensure patient safety and trial compliance, maintaining inspection readiness.
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Collaborate with Clinical Trial Assistants, Site Managers, and Global Trial Managers to ensure study delivery.
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Manage trial finances, ensuring accurate reporting and adherence to the budget.
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Contribute to quality control and corrective actions as needed, ensuring CAPA is implemented for audits/inspections.
Requirements:
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A BA/BS degree in a health or science-related field.
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More than 2 years of local trial management experience.
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Fluent in both Arabic and English.
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Experience in managing and starting complex Early Phase trials with internal clinical teams and sites.
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Strong focus on quality, compliance, and patient safety.
About the Company:
IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence. IQVIA accelerates the development and commercialization of innovative medical treatments to improve patient outcomes worldwide.
