IQVIA, a global leader in clinical research and healthcare intelligence, is hiring a Clinical Research Associate (CRA 2) for its Thane, Maharashtra location. This is an excellent opportunity for professionals with at least 1 year of on-site monitoring experience to advance their careers in clinical research.
Key Responsibilities
As a Clinical Research Associate (CRA), you will be responsible for:
- Conducting site monitoring visits (selection, initiation, monitoring, and close-out) in compliance with GCP, ICH guidelines, and sponsor requirements.
- Training site staff on study protocols and ensuring adherence to regulatory standards.
- Tracking study progress, including regulatory approvals, patient recruitment, and data reporting.
- Ensuring proper documentation in the Trial Master File (TMF) and Investigator’s Site File (ISF).
- Managing site relationships and resolving study-related issues efficiently.
- Supporting subject recruitment strategies to meet project timelines.
- Handling site financial management as per clinical trial agreements (if applicable).
Qualifications & Skills Required
- Bachelor’s degree in a scientific or healthcare-related field (preferred).
- Minimum 1 year of on-site monitoring experience in clinical research.
- Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
- Proficiency in Microsoft Office (Word, Excel, PowerPoint) and electronic data capture systems.
- Excellent communication, organizational, and problem-solving skills.
- Ability to manage time and site budgets effectively.
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 improving patient outcomes, IQVIA delivers intelligent healthcare solutions that accelerate drug development and commercialization.
How to Apply
Advertisement
