Healthcare Job Opportunity at IQVIA in Bengaluru | Apply Now
Looking for a rewarding healthcare job in clinical research? IQVIA is hiring an Associate Site Report Specialist in Bengaluru, India. This full-time, home-based role offers an excellent opportunity to work with a global leader in clinical research services while supporting high-impact clinical trials through data analysis, reporting, and regulatory compliance. This IQVIA job is ideal for professionals seeking growth through IQVIA careers in the life sciences sector.
Job Details:
- Job Title: Associate Site Report Specialist
- Location: Bengaluru, India
- Job ID: R1521194
About the Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The organization creates intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. This IQVIA job is part of the company’s commitment to excellence and integrity in healthcare research. Professionals exploring long-term growth through IQVIA careers will find strong global exposure and impactful work.
Qualifications
- Bachelor’s degree in a healthcare or other scientific discipline or its educational equivalent
- Minimum of 3 years of clinical research experience
- At least 2 years of on-site monitoring experience
- Knowledge of principles, theories, and concepts related to clinical research operations
- An equivalent combination of education, training, and experience may be considered
Job Description
The Associate Site Report Specialist role is a full-time, home-based healthcare job located in Bengaluru, India. The position provides project-related assistance for assigned projects, sites, and project teams. The role includes leading teams functionally where assigned, ensuring awareness of the scope of work, budget, and resources. All activities are conducted in accordance with SOPs, policies, good clinical practices, applicable regulatory requirements, and quality and timeline metrics. This position supports critical trial operations and contributes significantly to successful clinical study execution within jobs in Bengaluru.
Key Responsibilities
- Draft and update the study monitoring plan for sponsor studies and protocols
- Prepare, handle, distribute, file, and archive study-related logs and forms
- Assist with periodic review of study files for accuracy and completeness
- Support preparation, handling, and distribution of clinical trial supplies and tracking information
- Develop, prepare, and maintain global study performance dashboards
- Assist study teams during planning, maintenance, and close-out phases with data analysis and reporting
- Support risk mitigation for high-risk trials through detailed analytical reports
- Maintain accurate data updates in systems and tools within defined timelines
- Respond to information requests and resolve data discrepancies
- Identify and interpret trends and patterns across clinical metrics
- Design clinical and administrative reports
- Support eTMF activities, including filing, QC, and document classification
- Provide SME support, training, and systems expertise
- Review and finalize CRA reports using GCP and protocol knowledge
