CRA 2 at IQVIA – Thane/Ahmedabad | 1+ Years Experience Required | Apply by 10 September 2026
IQVIA CRA 2 Jobs offer a clinical research opportunity in Thane and Ahmedabad for candidates with on-site monitoring experience and a solid understanding of GCP and ICH guidelines. Interested candidates are encouraged to review the eligibility criteria and apply before the deadline of 10 September 2026.
About IQVIA
IQVIA is a global organization operating at the intersection of clinical research, healthcare intelligence, and pharmaceutical innovation. With a commitment to advancing healthcare through data-driven insights and technology, IQVIA collaborates with clients across the life sciences sector to improve patient outcomes and drive efficiency in clinical trials. The company is headquartered in Durham, North Carolina, and has a presence in numerous countries worldwide.
Job Details
Company: IQVIA
Job Role: CRA 2
Employment Type: Full-time
Locations: Thane, Maharashtra; Ahmedabad, India
Experience Required: Minimum 1 year of on-site monitoring experience
Qualification: Bachelor’s Degree in Scientific Discipline or Healthcare preferred
Job ID: R1564899
Posted Date: 09 September 2026
Application Deadline: 10 September 2026
Estimated Salary: ₹6–12 LPA*
IQVIA CRA 2 Jobs: Job Overview
The IQVIA CRA 2 Jobs role involves clinical site monitoring and site management activities to ensure clinical studies are conducted according to study protocols, sponsor requirements, applicable regulations, and industry guidelines. This role involves monitoring clinical trial sites, supporting subject recruitment, managing study documentation, tracking regulatory submissions, and ensuring compliance with Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines.
Key Responsibilities
- Conduct site selection, initiation, monitoring, and close-out visits.
- Ensure compliance with study protocols and regulatory requirements.
- Apply GCP and ICH guidelines during clinical trial monitoring.
- Support and track subject recruitment activities.
- Provide protocol and study-related training to assigned clinical sites.
- Maintain regular communication with investigators and site personnel.
- Evaluate study site practices and identify quality or compliance issues.
- Prepare monitoring visit reports and follow-up documentation.
Eligibility Criteria
- Bachelor’s Degree in a scientific discipline or healthcare-related field preferred.
- At least 1 year of on-site clinical monitoring experience.
- Knowledge of clinical research regulatory requirements.
- Strong understanding of GCP and ICH guidelines.
- Good therapeutic and protocol knowledge.
- Proficiency in Microsoft Word, Excel, and PowerPoint.
- Strong written and verbal communication skills.
- Effective time and financial management skills.
How to Apply
To apply for the CRA 2 position, please visit the following link: CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
Why Join IQVIA?
Professionals joining through IQVIA CRA 2 Jobs may have opportunities to work on innovative healthcare and pharmaceutical projects while collaborating with multidisciplinary teams. The organization offers exposure to clinical research, pharmaceutical innovation, and advanced AI and Machine Learning technologies, fostering professional development and career advancement across various sectors.
Note: The application deadline stated in the source notification may have passed. Verify before applying.
Conclusion
IQVIA CRA 2 Jobs are an excellent fit for qualified candidates seeking to advance their careers in clinical research. Interested individuals are encouraged to apply before the deadline of 10 September 2026 to ensure consideration for this role.
