IQVIA Hiring Clinical Research Associate (CRA) 2026 | Pharma Jobs in India (2+ Years Experience)
IQVIA Hiring Clinical Research Associate (CRA) 2026 | Pharma Jobs in India (2+ Years Experience)
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(IQVIA Hiring Clinical Research Associate (CRA) 2026) |
Introduction
The clinical research industry in India is growing rapidly, offering excellent career opportunities for professionals with experience in clinical trials and monitoring. One such high-value opportunity is now open at IQVIA for the position of Clinical Research Associate (CRA).
This role is ideal for candidates who already have on-site monitoring experience and want to take their careers to the next level in the CRO (Contract Research Organization) sector.
With exposure to global clinical trials, GCP compliance, and site management, this job provides a strong platform for long-term career growth in clinical research and drug development.
About The Company
IQVIA is a global leader in clinical research, healthcare analytics, and commercial solutions. The company is headquartered in Durham, North Carolina, US, and was formed in 2016 after the merger of IMS Health and Quintiles.
IQVIA operates in more than 100 countries and has over 85,000+ employees worldwide (2025 estimate). The company supports pharmaceutical, biotech, and healthcare organizations in conducting clinical trials, managing data, and improving patient outcomes.
In India, IQVIA has a strong presence across metro cities and is known for offering high-quality career opportunities in clinical research and data science.
Job Overview Summary
The Clinical Research Associate (CRA) role at IQVIA focuses on monitoring clinical trials and ensuring that studies are conducted according to regulatory guidelines and protocols.
This position requires candidates to perform onsite monitoring visits, verify clinical data, and coordinate with investigators and sponsors. It is a field-based role that involves frequent interaction with clinical trial sites.
Candidates will gain valuable experience in clinical operations, regulatory compliance, and trial execution.
Vacancy Details (Official)
- Company: IQVIA
- Role: Clinical Research Associate (CRA)
- Location: Metro Cities, India
- Experience: Minimum 2+ Years
- Job Type: Full-Time
- Application Mode: Email
Responsibility Explanation
As a CRA, your primary responsibility will be to ensure that clinical trials are conducted properly at different sites.
You will visit hospitals or research centers to monitor study progress, check patient data, and verify that the study is being conducted according to the approved protocol.
You will also identify any issues, es such as protocol deviations or data discrepancies, and work with site staff to resolve them. Preparing detailed reports after each visit is also an important part of the job.
Overall, you will act as a bridge between sponsors and clinical trial sites, ensuring quality, compliance, and smooth trial execution.
Eligibility (Official)
- Minimum 2+ years of onsite monitoring experience
- Must have completed 80+ onsite interim monitoring visits
- Strong understanding of clinical trial processes and GCP
Required Qualifications (Official)
- B.Pharm / M.Pharm / Pharm.D
- BHMS / BAMS / BDS
- Life sciences or clinical background candidates eligible
Skills Required
To succeed in this role, candidates must have strong knowledge of ICH-GCP guidelines and clinical trial monitoring processes.
Good communication skills are essential because you will interact with investigators, sponsors, and site teams. You should also have strong attention to detail for data verification and documentation.
Time management and problem-solving skills are also important, as you will handle multiple sites and responsibilities simultaneously.
Salary Estimate
The estimated salary for IQVIA CRA roles in India is:
₹6 LPA – ₹12 LPA
This may vary based on experience, number of monitoring visits completed, and overall expertise in clinical research.
Interview Details (Official)
- Interview Mode: Online / Virtual
- Selection Process: Resume screening + Technical Interview + HR Round
Required Documents
Candidates should keep the following documents ready:
- Updated Resume (CV)
- Educational Certificates
- Experience Certificates
- Monitoring Visit Proof (if available)
- Identity Proof (Aadhaar/PAN)
- Passport-size Photograph
How to Apply
Interested candidates can apply by sending their updated CV to:
📧 ashwini.veerabhadrappa@iqvia.com
Make sure to mention “Application for CRA Position” in the subject line.
FAQs Section
Q1. What is the role of a CRA in IQVIA?
A CRA monitors clinical trials, ensures compliance, and verifies patient data at trial sites.
Q2. Can freshers apply for this job?
No, this role requires at least 2 years of onsite monitoring experience.
Q3. What is SDV in clinical research?
SDV stands for Source Data Verification, which ensures the accuracy of clinical trial data.
Q4. What is the salary for CRA in IQVIA?
The salary ranges from ₹6 LPA to ₹12 LPA depending on experience.
Q5. Is this a field job?
Yes, CRA roles involve site visits and monitoring activities.
Final Conclusion
The IQVIA Clinical Research Associate (CRA) role is a high-growth opportunity for experienced professionals in clinical research.
With strong exposure to global clinical trials, regulatory compliance, and monitoring operations, this job can significantly boost your career in the CRO industry.
If you already have monitoring experience and want to work with a global leader like IQVIA, this opportunity is definitely worth applying for.
Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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