Are you a Clinical Research Professional looking for an exciting opportunity in Bangalore? IQVIA is hiring a Clinical Process Coordinator with 1-2 years of experience in clinical trials. If you have a background as a Clinical Trial Associate (CTA), CRC, or Clinical Trial Assistant, this could be your next career move!
Job Description: Clinical Process Coordinator
Key Responsibilities:
- Assist in the coordination and execution of clinical trial processes
- Support site management, data collection, and regulatory documentation
- Work closely with clinical research teams to ensure compliance with protocols
- Maintain trial master files (TMF) and ensure proper documentation
- Facilitate communication between investigators, sponsors, and clinical teams
- Ensure adherence to ICH-GCP guidelines and SOPs
Eligibility Criteria:
- 1-2 years of experience in Clinical Trial Associate (CTA), CRC, or Clinical Trial Assistant roles
- Strong understanding of clinical research processes & regulatory requirements
- Excellent communication and organizational skills
- Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field
About IQVIA
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 healthcare intelligence, IQVIA helps biotech and pharmaceutical companies accelerate drug development and improve patient outcomes.
Why Join IQVIA?
✅ Global exposure in clinical research
✅ Hybrid work model (Work from Home + Office)
✅ Career growth opportunities in a Fortune 500 company
✅ Competitive salary & benefits
How to Apply?
If you meet the eligibility criteria, send your updated resume to:
📩 navitha.gouli@iqvia.com
Subject Line: “Application for Clinical Process Coordinator – Bangalore”