IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. With a focus on innovation and data-driven insights, IQVIA helps biotech, pharmaceutical, and healthcare organizations accelerate advancements in patient care.
Job Overview
The Lab Cent Project Coordinator 1 will manage assigned monitoring responsibilities for clinical trials, ensuring timely and high-quality execution of tasks. This role involves centralized monitoring activities, regulatory documentation, and coordination with cross-functional teams.
Key Responsibilities
- Perform centralized monitoring activities for assigned projects under minimal supervision.
- Complete role-specific trainings (self-learning, instructor-led, e-SOPs) on time.
- Maintain active databases with site participation details.
- Manage Infosario Portal access provisioning.
- Ensure timely completion of regulatory documentation (Kit Contents Chart, Packing List, Import Permit).
- Monitor patient lab report releases by coordinating with relevant teams.
- Maintain audit-ready documentation for all monitoring activities.
- Participate in process improvement initiatives as needed.
Qualifications & Skills
- Preferred: B.Sc/M.Sc freshers.
- Basic knowledge of systems and procedures through prior experience or education.
- Ability to comply with company standards and regulations.
- Strong critical thinking and problem-solving skills.
- Excellent written and verbal communication (English proficiency required).
- Proficient in Microsoft Office (Word, Excel).
- Ability to work in a fast-paced, high-stress environment.
- Strong interpersonal and organizational skills.
Why Join IQVIA?
- Work with a global leader in clinical research.
- Opportunities for career growth and skill development.
- Collaborative and dynamic work environment.
How to Apply
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