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Job Description
- Req#: 299115
- Responsible for and/or contributes to the timely and quality delivery of coded terms (for Adverse events, concomitant medications, medical histories, medical procedures, etc.) and effective usage of medical and drug terminology, for clinical trials, pharmacovigilance, post-marketing safety surveillance, and other databases.
2. Assisting with the maintenance of the coding dictionaries and infrastructure (IT tools, documentation) needed to support coding and ensuring their consistency and validity across the corporation.
3. Providing basic coding consultancy for clinical trials, pharmacovigilance, post-marketing safety surveillance, and other business areas at the study level
4. Contribute to study milestones and deliverables : Has a basic understanding of the disease progression for the studies they are responsible for, with a view to understanding the data collection and reporting needs.
5. Able to identify coding related system problems and triage to the appropriate support teams. Maintains awareness of changes in regulatory requirements attending industry meetings and external user groups when necessary. Able to use sophisticated technical tools e.g. batch autoencoder, Veeva Coder, RAVE coder.
6. Study level management: Assure the timely and quality delivery of coded terms, for adverse events, concomitant medications, medical histories, medical procedures, and other approved coded forms for studies that they have responsibility for according to and industry expectations.
7. Oversee coding performed at the study level for studies. Able to perform coding query management tasks in EDC/clinical data capture systems. Resolve technical and process related coding issues.
About the company
Tata Consultancy Services is an Indian multinational information technology services and consulting company headquartered in Mumbai, Maharashtra, India with its largest campus located in Chennai, Tamil Nadu, India.
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