
About Me
1. Clinical Data Standards professional with Overall experience 18 years 8 months in Data Management.
2. Hands on experience in SAS Programming and Data Management support for Phase 1 IV trials.
3. Sound understanding of clinical trial practices, procedures and methodologies.
4. Ensures consistency of clinical data and processes across clinical trials and in compliance with regulatory requirements.
5. Supervised Programming team for many Phase I IV trials and I was successful in maintaining quality, productivity and timelines of the project
6. Supervised Data Coding Activities from Programming side.
7. Contributes to the Clinical Data Management team as an individual contributor who is a developing subject matter expert, who works independently with minimal supervision and who takes a leadership role in the collaboration with various internal and external partners.
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