IQVIA, a global leader in clinical research services and healthcare intelligence, is hiring for Site Solutions Associate and Associate Site Report Specialist (SVR Review) roles across India. These IQVIA clinical research jobs are ideal for professionals seeking career growth in clinical trial payments, site management, site monitoring review, and GCP compliance.
With opportunities in Bangalore, Thane, Hyderabad, Kolkata, and Ahmedabad, this is a strong career move for candidates looking to work in global CRO operations, clinical trial oversight, and regulatory-compliant study execution.
1️⃣ Site Solutions Associate – Bangalore
Job Overview
The Site Solutions Associate at IQVIA is responsible for clinical trial site communication, contract documentation validation, site payment processing, and compliance with SSAE18 policies. This role supports the financial and administrative lifecycle of clinical trials from study start-up through closeout.
Key Responsibilities
- Support clinical trial start-up, maintenance, and study closeout payment activities
- Maintain master site list and site documentation (CTA, W9, W8, PIF, amendments)
- Process site payments and pass-through payments accurately and timely
- Interpret and implement Clinical Trial Agreements (CTAs)
- Ensure SSAE18 compliance in payment and vendor setup processes
- Manage site administrative trackers and issue resolution
- Provide status updates for Sponsor Governance Meetings
- Act as escalation point for site-specific operational issues
Required Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, or related field
- Experience in clinical trial payments, contracts, or site administration preferred
- Strong understanding of clinical trial documentation and compliance
- Excellent communication and stakeholder coordination skills
- Attention to detail and process improvement mindset
Salary (Estimated)
💰 ₹4.5 – ₹8 LPA (approx.)
2️⃣ Associate Site Report Specialist (SVR Review) – PAN India
📍 Locations: Bangalore, Thane, Hyderabad, Kolkata, Ahmedabad
Job Overview
The Associate Site Report Specialist at IQVIA reviews Site Visit Reports (SVRs) to ensure compliance with ICH-GCP, IQVIA SOPs, and protocol requirements. This is a senior-level clinical research quality oversight role with strong monitoring expertise.
Key Responsibilities
- Review Site Visit Reports (SVRs) for protocol and GCP compliance
- Identify trends and escalate CRA or site issues
- Ensure corrective/preventive action plans are documented and tracked
- Support Clinical Project Managers (CPMs) with SVR insights
- Conduct compliance tracking and quality improvement activities
- Mentor CRAs and junior team members
- Participate in project meetings and governance discussions
Required Qualifications
- Bachelor’s degree in Healthcare or Life Sciences
- 7–8 years clinical research experience
- Minimum 3–4 years on-site monitoring experience
- Strong knowledge of ICH-GCP and regulatory requirements
- Excellent analytical, communication, and organizational skills
Salary (Estimated)
💰 ₹10 – ₹18 LPA (approx.)
Why Join IQVIA?
- Work with a global clinical research organization
- Exposure to international sponsors and complex study designs
- Strong compliance-driven work culture
- Career growth in clinical operations and site management
- Opportunity to work across geographies and cultures
IQVIA is known for its excellence in clinical research services, regulatory compliance, and healthcare data intelligence.
How to Apply
Application Link For Site Solutions Associate – Bangalore
Application Link For Associate Site Report Specialist (SVR Review) – PAN India
