Specialist Jobs at IQVIA – Associate Site Report Specialist Role | Clinical Research Jobs | Apply Now
IQVIA is hiring for one of its most impactful Specialist Jobs in India. This Associate Site Report Specialist role is a home-based opportunity designed for professionals seeking long-term growth in Clinical Research Jobs. As part of IQVIA Jobs, you will support global clinical trials, ensure GCP compliance, and deliver high-quality reporting and data insights across study teams.
- Job Title: Associate Site Report Specialist
- Location: Thane, India
- Job ID: R1521194
About the Company:
IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence. Through innovation, data science, and deep therapeutic expertise, IQVIA Jobs empower professionals to accelerate the development of medical treatments that improve patient outcomes worldwide.
Job Overview:
The Associate Site Report Specialist provides project-related assistance to assigned studies, sites, and teams. This role supports planning, execution, maintenance, and close-out activities while ensuring work is conducted in accordance with SOPs, GCP, and regulatory requirements. It is one of the most structured Specialist Jobs within Clinical Research Jobs, focusing on data accuracy, reporting, and stakeholder coordination.
Key Responsibilities:
- Draft and update study monitoring plans for sponsor protocols
- Prepare, manage, and archive study-related logs and documentation
- Assist in periodic review of study files for accuracy and completeness
- Support clinical trial supply tracking and documentation
- Develop and maintain global study performance dashboards
- Provide analytical reports for study planning, maintenance, and close-out
- Support risk mitigation through detailed data analysis
- Maintain clinical data in systems and tools within defined timelines
- Resolve data discrepancies and respond to stakeholder queries
- Assist in eTMF filing, QC, and document classification
- Review and finalize CRA reports within timelines using GCP knowledge
- Support audits, training initiatives, and quality improvement activities
Educational Requirements:
- Bachelor’s degree in Healthcare, Life Sciences, or related scientific discipline
- 3 years of Clinical Research experience, including a minimum of 2 years on-site monitoring experience and training.
Skills Required:
- Strong understanding of clinical trial operations and reporting
- Knowledge of GCP, SOPs, and regulatory requirements
- Experience with eTMF, CRFs, and clinical data flow
- Analytical mindset with ability to interpret trends and metrics
- Effective communication and stakeholder coordination skills
- Ability to support cross-functional clinical teams remotely
This role stands out among Specialist Jobs at IQVIA Jobs for professionals seeking stable, remote Clinical Research Jobs with global exposure. If you are passionate about data quality, compliance, and clinical operations, this opportunity offers both growth and impact.
