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IQVIA, a global leader in clinical research and healthcare intelligence, is actively hiring Clinical Research Associates (CRA) for metro city locations in India.
This opportunity is ideal for professionals with 2+ years of onsite monitoring experience who want to advance their careers in clinical trials, site management, and monitoring operations.
With strong exposure to interim monitoring visits, GCP compliance, and clinical trial execution, this role provides a high-growth pathway in the CRO industry.
Job Overview
- Position: Clinical Research Associate (CRA)
- Company: IQVIA
- Location: Metro Cities, India
- Experience: Minimum 2+ Years
- Qualification: B.Pharm / M.Pharm / Pharm.D / BHMS / BAMS / BDS
- Application Mode: Email
Key Responsibilities
- Conduct onsite monitoring visits (interim, initiation, close-out)
- Ensure compliance with ICH-GCP guidelines and regulatory requirements
- Perform source data verification (SDV) and data quality checks
- Maintain clinical trial documentation (TMF/eTMF)
- Coordinate with investigators, site staff, and sponsors
- Identify and resolve protocol deviations and site issues
- Prepare monitoring visit reports within defined timelines
Eligibility Criteria
- Minimum 2+ years of onsite monitoring experience
- Must have completed 80+ onsite interim monitoring visits
- Strong understanding of clinical trial processes and GCP
- Excellent communication and stakeholder management skills
Required Qualifications
- B.Pharm / M.Pharm / Pharm.D
- BHMS / BAMS / BDS (Life sciences/clinical background)
- Prior experience in clinical research / CRO environment preferred
Benefits of Working at IQVIA
- Opportunity to work with a global CRO leader
- Exposure to international clinical trials and sponsors
- Career growth in clinical operations and monitoring
- Competitive salary and performance-based incentives
- Learning & development in advanced clinical technologies
How to Apply
Interested candidates can apply by sending their updated CV to:
๐ง ashwini.veerabhadrappa@iqvia.com
Tip: Highlight your number of monitoring visits (80+), therapeutic area experience, and GCP knowledge clearly in your CV.
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