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IQVIA Hiring Freshers For Lab Cent Project Coordinator 1 in Clinical Research

Job Title: Lab Cent Project Coordinator

Location: Kochi, India

Application Deadline: August 9, 2025

Summary:

Are you a recent graduate or early-career professional with a passion for clinical research? IQVIA, a global leader in providing advanced analytics, technology solutions, and clinical research services to the life sciences industry, is seeking a highly motivated and detail-oriented Lab Cent Project Coordinator to join our team in Kochi. This is an excellent opportunity to gain hands-on experience in a dynamic and rewarding environment, contributing to cutting-edge medical advancements and improving patient outcomes worldwide. If you are eager to kickstart your career with a reputable organization and possess the required skills and qualifications, we encourage you to apply!

About IQVIA:

IQVIA is committed to driving healthcare forward. We partner with pharmaceutical, biotechnology, and healthcare organizations to accelerate the development of innovative therapies and improve patient access to life-saving treatments. Through our comprehensive suite of services, we empower our clients to make data-driven decisions, optimize clinical trials, and deliver better health outcomes.

Job Description:

As a Lab Cent Project Coordinator, you will be an integral part of our centralized monitoring team, responsible for managing critical aspects of clinical research projects. Your role will involve ensuring the smooth and efficient execution of laboratory-related activities, contributing directly to the success of clinical trials.

Responsibilities:

  • Complete all assigned role-specific training modules promptly, including self-learning courses, instructor-led sessions, and electronic Standard Operating Procedure (e-SOP)/Work Instruction (WI) acknowledgments.
  • Load and maintain accurate databases containing details of participating clinical trial sites.
  • Provision access to the Infosario Portal for authorized personnel.
  • Ensure timely and accurate preparation of regulatory documentation required for kit shipments, including Kit Contents Charts (KCC), Packing Lists, and Import Permits.
  • Proactively monitor and follow up on pending activities to ensure the on-time release of patient laboratory reports.
  • Maintain comprehensive and up-to-date documentation for real-time audit readiness.
  • Actively participate in departmental meetings and contribute to process improvement initiatives to enhance efficiency and quality.

Qualifications and Skills:

  • Education: High School Diploma or equivalent is required.
  • Experience: 0-1 year of prior work experience or education in related systems and procedures. Fresh graduates are encouraged to apply.
  • Skills:
    • Basic knowledge of relevant systems and procedures acquired through education or prior work experience.
    • Ability to adhere to company standards, protocols, and regulatory guidelines.
    • Exceptional multitasking abilities with demonstrated critical thinking and problem-solving skills.
    • Excellent written and verbal communication skills, with a strong command of the English language.
    • Strong interpersonal skills and the ability to build effective working relationships with colleagues and managers.
    • Exceptional organizational and time management skills to prioritize tasks and meet deadlines.
    • Proficiency in word processing and spreadsheet applications, such as Microsoft Word and Excel.
    • Ability to thrive in a fast-paced, high-pressure environment while maintaining accuracy and attention to detail.
    • A proactive and self-motivated approach to work, with the ability to work independently under minimal supervision.

Why IQVIA?

Joining IQVIA means becoming part of a world-class team dedicated to improving healthcare outcomes worldwide. We offer:

  • Professional Growth: Opportunities for skill development and career advancement within a dynamic and growing organization.
  • Impactful Work: The chance to contribute to innovative medical treatments and improve patient lives globally.
  • Collaborative Environment: A supportive and collaborative work environment where teamwork and innovation are valued.
  • Comprehensive Benefits: A competitive compensation and benefits package.
  • Global Leader: Be part of a global leader in clinical research and healthcare intelligence.

This entry-level role is a fantastic stepping stone for a rewarding career in the life sciences and healthcare industries. If you are a driven and dedicated individual with a passion for making a difference, we encourage you to apply!