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Novartis is a global healthcare leader and has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented, performance driven people. All of which makes us one of the most rewarding employers in our field. We appreciate and welcome your interest in joining our team of associates from more than 150 nationalities who currently share our mission to care and to cure. Our career website is updated regularly and can be viewed in other languages by selecting the option in the upper right corner.
| 201873BR | |
| Analyst – Clinical Coding | |
| Global Drug Development | |
| GDO GDD | |
| India | |
| Hyderabad | |
| Nov Hltcr Shared Services Ind | |
| Research & Development | |
| Full Time | |
| Regular |
Job Description :
- Performs accurate/consistent coding, applying standard conventions, creating ap-propriate synonyms, and creating/closing coding-related queries as needed
- Reviews/provides feedback on coding performed by self or others to ensure consistency and quality
- Reviews/provides feedback on synonyms
- Ensures that coding is completed in support of study team timelines/deliverables
- Maintains Coding-related section(s) of study DHPs (or equivalent documents)
- Troubleshoots coding problems, collaborating with peers, database developers, and/or IT support as needed
- Interacts with TDMs, CTH’s, Medics and other Clinical Trial Team members as ap-propriate to ensure the quality/completeness coded data
Minimum requirements
- University or college degree in life science, chemistry, pharmacy, nursing, or equivalent relevant degree
- English (oral and written)
- 3 or more years of experience in drug development with at least 2 years performing Clinical coding.
- Strong understanding of medical terminology, in-cluding medical conditions and medications
- Strong attention to detail.
- Good communication, problem-solving, negotiation and conflict resolution skills
- Ability to work independently, under pressure, and in an environment where flexibility is required.
- Understanding of clinical trials methodology, GCP and coding tools
