IQVIA, a global leader in clinical research and healthcare intelligence, is hiring an Associate Site Report Specialist for its India operations in Bangalore and Thane. This role is ideal for clinical research professionals with strong site monitoring, reporting, eTMF, and data analysis experience who want to work on global sponsor studies in a high-impact environment.
If you are seeking a career-defining opportunity in clinical operations, study reporting, and GCP-compliant trial execution, this position offers excellent exposure to cross-functional teams and global stakeholders.
🔍 Job Overview
As an Associate Site Report Specialist at IQVIA, you will provide project-level support across assigned clinical trials, sites, and project teams. The role involves study monitoring plans, clinical dashboards, report review, eTMF quality checks, and risk mitigation analysis, ensuring all activities meet SOPs, ICH-GCP, and regulatory requirements within defined timelines.
📌 Key Responsibilities
- Draft, update, and maintain Study Monitoring Plans
- Prepare, handle, file, and archive study logs and trial documentation
- Support eTMF filing, initial QC, classification, and detailed quality checks
- Review study files for accuracy, completeness, and compliance
- Develop and maintain global study performance dashboards
- Analyze clinical data trends, metrics, and risk indicators
- Assist project teams during planning, maintenance, and close-out phases
- Review and finalize CRA monitoring reports using GCP and protocol knowledge
- Support CRF tracking, query management, and clinical data flow
- Respond to data and information requests from internal and sponsor stakeholders
- Track monthly retrospective quality issues
- Act as a systems expert: create guidance documents and conduct trainings
- Collaborate with IT, clinical, and operational teams
- Support sponsor meetings and trial managers on study activities
- Advocate strict adherence to SOPs and quality standards
🎓 Qualifications & Experience
- Bachelor’s degree in Life Sciences, Pharmacy, Clinical Research, or related discipline
- 3+ years of clinical research experience
- Minimum 2 years of on-site monitoring experience
- Strong understanding of ICH-GCP, clinical operations, and regulatory requirements
- Experience with eTMF systems, CRFs, dashboards, and reporting tools
- Excellent analytical, documentation, and stakeholder communication skills
- Equivalent combination of education, training, and experience will be considered
💼 Salary & Benefits (Indicative)
- Salary Range: ₹6,00,000 – ₹9,00,000 per annum (INR)
- Opportunity to work with a global CRO leader
- Exposure to international sponsor studies
- Structured training and career development programs
- Strong compliance, quality, and ethics-driven work culture
- Inclusive and collaborative work environment
📝 How to Apply
