IQVIA is hiring for the role of Clinical Process Coordinator in Bangalore. This is an excellent opportunity for professionals with 6 months to 1 year of experience in clinical research, CTA (Clinical Trial Assistant), CRC (Clinical Research Coordinator), or clinical trials.
Key Responsibilities:
- Manage visit tracking in CTMS for Investigator payments.
- Handle Vendor Setup QCs, PV Batch Review, and Passthrough invoice Batch Review.
- Provide and revoke system access as required.
- Review ATP (Authorization to Proceed) trainings.
- Coordinate with translation vendors.
- Ensure compliance with contracts and maintain high-quality output for processing teams.
Required Skills & Qualifications:
- 0-1 years of experience in clinical research or related fields.
- Knowledge of clinical trial processes, CTA, CRC, or clinical research coordination.
- Strong organizational and communication skills.
- Ability to work in a hybrid model (office-based in Bangalore).
About IQVIA
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. With a strong reputation in clinical trials and healthcare intelligence, IQVIA helps biotech, pharmaceutical, and medical device companies improve patient outcomes worldwide.
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🌟 Why Join IQVIA?
- Work with a top-rated employer (3.8/5 Glassdoor reviews).
- Gain exposure to global clinical research projects.
- Hybrid work model for better work-life balance.
- Career growth opportunities in the clinical research domain.
How to Apply?
