Medical Data Reviewer Role at ICON in Bangalore | Remote Clinical Research Role | Apply Online!!
Are you a healthcare professional with expertise in clinical data review? ICON, the world’s largest and most comprehensive clinical research organization, is seeking a Medical Data Reviewer to join our team remotely in Bangalore. This role offers the opportunity to work in clinical monitoring, ensuring the accuracy of medical data while contributing to groundbreaking research. If you have a background in MD, PharmD, PhD, or Nursing and experience in Solid Tumor Oncology, apply today and be part of a team shaping the future of healthcare intelligence.
About ICON
ICON is the world’s largest and most comprehensive clinical research organization, dedicated to advancing healthcare through innovative research and data-driven solutions. With a global presence, ICON partners with leading pharmaceutical, biotechnology, and medical device companies to drive groundbreaking clinical trials that improve patient outcomes. Powered by healthcare intelligence, ICON provides cutting-edge clinical monitoring, data management, and regulatory support, ensuring the highest standards of quality and efficiency. Committed to excellence, ICON fosters a diverse and dynamic work culture, empowering professionals to shape the future of medicine.
Job Details
- Job Title: Medical Data Reviewer
- Location: Bangalore
- Job Req ID: 2025-117881
- Department: Clinical Monitoring, ICON Strategic Solutions
- Job Type: Remote
About the role
What you will be doing as a Medical Data Reviewer Role:
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- Serve as a Clinical Data reviewer and identify any errors in data by performing a data review that requires further clarification with the study site.
- Perform ongoing review of clinical/medical aspects of assigned patient data and documents (escalates to Regeneron Clinical Scientist and/or medical monitor, as appropriate)
- Communicates any data training needs for CRAs, sites, etc.
- Conduct in-stream data trend analysis in support of data quality and integrity (includes protocol compliance and targeted review of patient data)
- Provide clinical data, Project Management, and viewed as an expert in data clinical/medical review and cleaning.
- Ensure data quality, focus on audit readiness with Clinical Compliance and Systems Validation Compliance.
- May assist in review and contribute to data capture requirements guidance in line with protocol and reporting requirements.
- Monitor site data entry performance and provide leadership to identify root causes of data issues and implement remedial actions.
- Ensure timely follow-up and resolution of data-related compliance issues.
- Continuously assess opportunities to improve the efficiency of tasks and the quality of data deliverables. May contribute to EDC completion training.
- May participate in clinical data review meetings such as:
- May be involved in preparing or reviewing material for and presenting in data dissemination meetings, such as: Investigator meetings, advisory boards, safety cohort review meetings, IDMC, SC, senior management meetings, central imaging review, CST/SPT/DPR/PRC discussions for study/program decisions
- May be involved in review and QC of clinical data sections for abstracts/manuscripts/ oral and poster presentations
- Will collaborate closely with Regeneron Clinical Scientists, Medical Directors, Data Management, and Clinical Operations to execute clinical data reviews and activities prior to data cuts for snapshots, interim analysis, DSUR, IBs, regulatory requests, study site close-outs, and final DBL.
- May be closely involved in data review and identification of readiness for clinical narratives for Clinical Study Report (CSR)
- May be involved in QC review of patient narratives and contribute to tracking of such.
You are:
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- Educational scientific background, such as MD, PharmD, PhD, Nursing degree, MSc
- ≥ 5 years of pharmaceutical clinical/medical data review experience is required, including clinical cross-check experience. 8+ years is preferable.
- Experience with Solid Tumor Oncology
- Excellent verbal and writing communication in English, organization, and tracking skills. Strong operational skills and demonstrated ability to meet timelines.
- Detail oriented
- Experience in coding review
- Query writing training
- Strong clinical database navigation skills
- Strong MS Excel, project management
- Proven ability to work independently and in a team setting.
- Knowledge of Good Clinical Practice; comprehensive knowledge of clinical trial design; understanding of the overall drug development process
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work-life balance opportunities for you and your family.
Our benefits examples include:
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- Various annual leave entitlements.
- A range of health insurance offerings to suit you and your family’s needs.
Keywords: Medical Data Reviewer, ICON, Bangalore, Clinical Monitoring, Healthcare, Remote Job
