IQVIA is hiring Clinical Research Associate (CRA 1/2) professionals for its Thane, Maharashtra office. This is an excellent opportunity for experienced clinical research professionals who have at least 1 year of on-site monitoring experience and want to build a long-term career with one of the world’s leading Clinical Research Organizations (CROs).
If you have experience in site monitoring, GCP compliance, investigator site management, TMF documentation, and clinical trial monitoring, this IQVIA CRA opportunity could be your next career move.
Job Overview
- Company: IQVIA
- Job Title: CRA 1/2 (Clinical Research Associate)
- Location: Thane, Maharashtra, India
- Job Type: Full-Time
- Experience: Minimum 1 Year On-site Monitoring Experience
- Qualification: Bachelor’s Degree in Life Sciences or Healthcare (Preferred)
- Application Deadline: 06 August 2026
- Job ID: R1557317
Key Responsibilities
As a Clinical Research Associate (CRA) at IQVIA, you will be responsible for monitoring clinical trial sites while ensuring regulatory compliance and high-quality study execution.
Responsibilities include:
- Conduct Site Selection Visits (SSV), Site Initiation Visits (SIV), Monitoring Visits (MV), and Close-Out Visits (COV)
- Ensure compliance with ICH-GCP guidelines, study protocols, and sponsor requirements
- Monitor patient recruitment and enrollment activities
- Support investigator sites with protocol implementation and study training
- Review CRFs and manage data query generation and resolution
- Track regulatory submissions and study approvals
- Ensure Investigator Site File (ISF) and Trial Master File (TMF) documentation are complete and inspection-ready
- Prepare monitoring visit reports and follow-up letters
- Escalate protocol deviations and quality issues when required
- Collaborate with sponsors, study teams, investigators, and site staff
- Support clinical trial startup activities where applicable
- Assist with clinical trial site financial management if assigned
Required Qualifications
Candidates should possess:
- Bachelor’s Degree in Life Sciences, Pharmacy, Biotechnology, Nursing, Medicine, or related healthcare discipline
- Minimum 1 year of on-site CRA monitoring experience
- Strong understanding of:
- ICH-GCP Guidelines
- Clinical Trial Regulations
- Site Monitoring
- Clinical Trial Protocols
- CRF Review
- TMF & ISF Documentation
- Regulatory Compliance
- Good communication skills in English
- Microsoft Word, Excel, PowerPoint proficiency
- Strong organizational and problem-solving abilities
- Ability to travel for site monitoring visits
Preferred Skills
- Clinical Trial Monitoring
- Investigator Management
- Subject Recruitment Support
- Clinical Documentation
- Risk Identification
- Protocol Compliance
- Site Management
- Query Resolution
- Time Management
- Sponsor Communication
Why Join IQVIA?
Joining IQVIA offers professionals an opportunity to work on global clinical research projects while advancing their CRA career.
Benefits include:
- Opportunity to work with one of the world’s leading CROs
- Exposure to international clinical trials
- Career progression from CRA I to Senior CRA and Clinical Trial Manager
- Global learning and development programs
- Collaborative work environment
- Competitive salary and employee benefits
- Experience across multiple therapeutic areas
Who Can Apply?
Suitable candidates include professionals with:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Microbiology
- Biochemistry
- Nursing
- Medical and Healthcare-related degrees
Note: This position requires minimum one year of on-site clinical monitoring experience.
How to Apply
