IQVIA Careers has announced new openings for SSU CRA (Site Start-Up Clinical Research Associate) positions in Thane, Maharashtra. Candidates with experience in clinical trial monitoring, GCP compliance, and site management can apply for this exciting opportunity in the clinical research industry.
This IQVIA SSU CRA job is ideal for candidates looking to build a long-term career in clinical research, clinical operations, site monitoring, and CRA roles in India.
About IQVIA
IQVIA Official Website is a global leader in clinical research services, healthcare intelligence, and commercial insights for the life sciences industry. The company supports pharmaceutical, biotechnology, and healthcare organizations worldwide through innovative clinical trial solutions and data-driven healthcare technologies.
Job Details
| Particulars | Details |
|---|---|
| Job Role | SSU CRA (Site Start-Up Clinical Research Associate) |
| Company | IQVIA |
| Location | Thane |
| Job Type | Full-Time |
| Experience Required | Minimum 1 Year |
| Qualification | Bachelorโs Degree in Scientific Discipline or Healthcare |
| Industry | Clinical Research |
| Last Date to Apply | May 14, 2026 |
| Job Requisition ID | R1541674 |
Primary Keywords
- IQVIA SSU CRA Jobs 2026
- Clinical Research Associate Jobs in Thane
- CRA Jobs in Maharashtra
- IQVIA Clinical Research Jobs
- Site Monitoring Jobs in India
- Clinical Trial Monitoring Jobs
- GCP Clinical Research Jobs
- Clinical Research Careers India
Job Responsibilities
Candidates selected for the IQVIA SSU CRA role will be responsible for:
- Conducting site monitoring visits including initiation, monitoring, and close-out visits
- Ensuring compliance with ICH-GCP guidelines and study protocols
- Managing subject recruitment and enrollment activities
- Supporting regulatory submissions and approvals
- Reviewing CRFs, data queries, and study documentation
- Maintaining Trial Master File (TMF) and Investigator Site File (ISF)
- Preparing monitoring reports and follow-up documentation
- Coordinating with investigators, study coordinators, and project teams
- Supporting site financial management where applicable
- Identifying and escalating quality or compliance issues
Required Qualifications
Applicants should meet the following eligibility criteria:
- Bachelorโs Degree in Life Sciences, Pharmacy, Healthcare, or related scientific discipline
- Minimum 1 year of on-site monitoring experience as CRA
- Good understanding of:
- ICH-GCP guidelines
- Clinical trial regulations
- Site management processes
- Protocol compliance
- Strong communication and documentation skills
- Knowledge of Microsoft Word, Excel, and PowerPoint
- Ability to manage timelines, study activities, and site coordination
Preferred Skills
- Clinical trial monitoring experience
- Regulatory documentation handling
- Problem-solving and organizational skills
- Effective communication with investigators and sponsors
- Experience in recruitment tracking and site management
Salary & Benefits
The expected salary for the IQVIA SSU CRA role in India may range between โน5 LPA to โน9 LPA, depending on experience, therapeutic expertise, and monitoring exposure.
Employee Benefits May Include:
- Global clinical research exposure
- Career growth opportunities
- Professional training programs
- Health and insurance benefits
- Flexible and collaborative work culture
- Opportunities to work on multinational clinical studies
Why This IQVIA CRA Job is Important
The demand for experienced Clinical Research Associates in India continues to grow due to increasing clinical trials and global pharmaceutical investments. IQVIAโs SSU CRA role offers strong exposure to:
- Clinical operations
- Regulatory compliance
- Site monitoring
- Trial management
- Global clinical research standards
Candidates with pharmacy, life sciences, or healthcare backgrounds can significantly strengthen their clinical research careers through this opportunity.
How to Apply
