IQVIA is a global leader in clinical research, healthcare intelligence, and commercial insights, dedicated to accelerating the development and commercialization of innovative medical treatments. With a strong presence in over 100 countries, IQVIA helps pharmaceutical, biotech, and medical device companies improve patient outcomes through data-driven solutions and advanced analytics.
๐ Learn more about IQVIA: https://jobs.iqvia.com
Job Description
As a Lab Centralized Project Coordinator at IQVIA, you will manage assigned monitoring responsibilities (including simple protocols and non-protocol tasks) efficiently while ensuring timeliness and quality.
Key Responsibilities:
โ Perform centralized monitoring activities for assigned projects under minimal supervision.
โ Complete role-specific trainings (self-learning, instructor-led, e-SOPs) on time.
โ Maintain and update active databases with site participation details.
โ Manage Infosario Portal access provisioning.
โ Ensure timely completion of regulatory documentation for kit shipments (KCC, Packing List, Import Permit).
โ Monitor on-time release of patient lab reports by coordinating with relevant teams.
โ Maintain real-time audit readiness by ensuring proper documentation.
โ Participate in process improvement initiatives as needed.
Qualifications & Skills Required
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Education: High School Diploma or equivalent (required).
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Experience: 0-1 year in a related field.
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Basic knowledge of systems and procedures.
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Strong critical thinking and problem-solving skills.
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Excellent written & verbal communication (English proficiency required).
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Proficient in Microsoft Office (Word, Excel).
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Ability to work in a fast-paced, high-stress environment.
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Strong interpersonal, organizational, and time management skills.
Why Join IQVIA?
โ Global leader in healthcare intelligence & clinical research.
โ Career growth opportunities in a dynamic work environment.
โ Competitive salary & benefits.
โ Inclusive workplace culture fostering innovation.
How to Apply?
๐ Donโt miss this opportunity! Apply before June 25, 2025.
