IQVIA is seeking a Clinical Research Coordinator in Bangalore to support clinical trials by performing data collection, patient recruitment, and regulatory compliance tasks. The role involves working closely with investigators to ensure adherence to Good Clinical Practice (GCP) and study protocols.
Key Responsibilities
- Review study protocols, Case Report Forms (CRFs), and regulatory documents.
- Recruit, screen, and orient patients for clinical trials.
- Conduct study visits, perform clinical procedures (ECG, spirometry, sample collection, etc.), and maintain source documentation.
- Ensure data accuracy and compliance with SOPs and FDA/regulatory guidelines.
- Monitor patient safety and report adverse events.
- Assist in training site staff and preparing for audits/inspections.
- Coordinate lab logistics and specimen handling.
Qualifications & Skills
- Bachelor’s Degree or High School Diploma with relevant experience.
- 3+ years in a clinical setting (medical assistant, lab technician, etc.).
- Knowledge of GCP, clinical trials, and regulatory requirements.
- Proficiency in MS Office (Word, Access, Outlook).
- Strong attention to detail and interpersonal skills.
- Certifications as per regulatory requirements.
About IQVIA
IQVIA is a global leader in clinical research, healthcare analytics, and commercial solutions for the life sciences industry. We accelerate medical innovation by providing intelligent insights and clinical trial expertise to improve patient outcomes worldwide.
How to Apply
📌 Last Date: June 14, 2025
📍 Location: Bangalore, India
