The IQVIA Centralized Site Associate job focuses on supporting clinical trial sites while ensuring compliance with ICH-GCP guidelines and regulatory standards. Candidates with an interest in clinical trials, site coordination, and remote study support should not miss this opportunity.
Job Details – Centralized Site Associate (IQVIA)
- Company: IQVIA
- Job Role: Centralized Site Associate
- Location: Thane, Maharashtra
- Experience Required: 0 years (Freshers eligible)
- Employment Type: Full Time, Permanent
- Industry: Pharmaceutical & Life Sciences
- Department: Healthcare & Life Sciences
- Openings: 1
- Posted On: January 9, 2026
Key Responsibilities
As a Centralized Site Associate at IQVIA, the selected candidate will be responsible for:
- Supporting clinical trial sites through centralized and remote activities
- Ensuring compliance with ICH-GCP, SOPs, and regulatory requirements
- Assisting in site document collection, review, and tracking
- Coordinating with investigators and site staff to resolve study-related queries
- Supporting clinical monitoring teams with site readiness activities
- Maintaining accurate clinical trial documentation and records
- Participating in audit and inspection readiness activities
Eligibility Criteria & Qualifications
To be eligible for the IQVIA Centralized Site Associate role, candidates must meet the following criteria:
Educational Qualification
- UG: B.Pharm or B.Sc (Life Sciences or related disciplines)
- PG (Preferred): M.Pharm or M.Sc (Science)
Skills & Knowledge
- Basic understanding of clinical research processes
- Knowledge of ICH-GCP guidelines
- Strong documentation and communication skills
- Ability to work in a regulated clinical research environment
- Attention to detail and compliance mindset
Salary & Benefits
- Expected Salary Range: ₹3,50,000 – ₹5,50,000 per annum (INR)
- Performance-based growth opportunities
- Exposure to global clinical trials
- Structured training and career development at IQVIA
- Work with one of the world’s most trusted CROs
Why Join IQVIA?
IQVIA is recognized globally for its innovation in clinical research, data analytics, and healthcare intelligence. Working as a Centralized Site Associate provides early exposure to global clinical trial operations, making it an excellent stepping stone for roles such as Clinical Research Associate (CRA), Site Manager, or Trial Operations Specialist.
How to Apply
Share Your Resumes on imran.patel2@iqvia.com
