Clinical Research Associate Job at IQVIA for metro cities India. Apply via email with 2+ years experience in monitoring.
Introduction
A leading opportunity has opened for experienced clinical research professionals who are looking to grow in monitoring and site management roles. This position is ideal for candidates with hands-on onsite monitoring experience who want to work on global clinical trials. If you are aiming for career advancement in the CRO industry, this role offers strong exposure and long-term growth potential.
Company Overview
IQVIA is a globally recognized contract research organization (CRO) that provides clinical research services, healthcare analytics, and commercial insights. The company plays a key role in accelerating drug development and improving healthcare outcomes worldwide. Professionals working at IQVIA gain exposure to international trials, advanced technologies, and global regulatory standards.
Job Location & Employment Type
- Location: Metro Cities across India
- Employment Type: Full-Time
- Work Setup: Field-based / Onsite Monitoring
Open Positions / Department Details
- Position: Clinical Research Associate (CRA)
- Department: Clinical Operations / Monitoring
- Experience Level: Mid-Level
Job Overview (Quick Details Table)
| Category | Details |
|---|---|
| Job Role | Clinical Research Associate (CRA) |
| Company | IQVIA |
| Location | Metro Cities, India |
| Qualification | B.Pharm / M.Pharm / Pharm.D / BHMS / BAMS / BDS |
| Experience | Minimum 2+ Years |
| Job Type | Full-Time |
| Industry | Clinical Research / CRO |
| Application Mode | |
| Job Type | Verified Job |
Key Roles & Responsibilities
As a Clinical Research Associate, you will be responsible for monitoring clinical trials and ensuring compliance with regulatory standards and study protocols.
- Conduct onsite monitoring visits including site initiation, interim, and close-out visits
- Ensure adherence to ICH-GCP guidelines and regulatory requirements
- Perform Source Data Verification (SDV) and ensure data accuracy
- Maintain Trial Master File (TMF/eTMF) documentation
- Coordinate with investigators, site staff, and sponsors
- Identify protocol deviations and implement corrective actions
- Prepare and submit monitoring visit reports within timelines
- Support overall clinical trial execution and site performance
Eligibility Criteria
Education
- B.Pharm / M.Pharm / Pharm.D
- BHMS / BAMS / BDS (Life sciences or clinical background)
Experience
- Minimum 2+ years of onsite monitoring experience
- Must have completed 80+ onsite interim monitoring visits
Skills Required
- Strong understanding of clinical trial processes
- Knowledge of ICH-GCP guidelines and regulatory compliance
- Excellent communication and stakeholder management skills
- Ability to handle multiple sites and projects efficiently
- Strong analytical and problem-solving abilities
Salary & Benefits
- Salary: As per company norms (competitive package expected)
- Performance-based incentives
- Opportunity to work on international clinical trials
- Career growth in clinical operations and monitoring roles
- Learning opportunities in advanced clinical technologies
Selection Process
The hiring process may include:
- Email application submission
- Resume shortlisting
- Technical/functional interview
- HR discussion
- Final selection
How to Apply
- Interested candidates should apply via email
- Send your updated CV to: ashwini.veerabhadrappa@iqvia.com
- Mention your monitoring experience, number of visits, and therapeutic areas clearly in your CV
Important Dates
- Application Deadline: Not specified (Apply as soon as possible)
Why Apply for This Pharma Job?
This role is a strong career move for experienced CRAs looking to work with a global CRO leader. It provides extensive exposure to clinical trial monitoring, regulatory compliance, and multi-site coordination. Candidates will gain hands-on experience with international sponsors and advanced clinical systems. The role also offers significant growth opportunities in clinical operations, making it ideal for professionals aiming for senior CRA or project management roles in the future.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with any company or recruiter. We share job information for educational and informational purposes only. Candidates are advised to verify details from official sources before applying. We do not charge any fees.
Final Call-to-Action
Eligible candidates with relevant monitoring experience should apply immediately via email to avoid missing this excellent opportunity in clinical research.
