Associate Senior Clinical Data Scientist
INR 900K-1250K (estimate) Mid-level Full Time
Tasks
- Collaborate with CROs and regulatory authorities
- Create Define.xml
- Create TFLs
- Create metadata specifications
- Develop data flow plans
- Develop eCRFs
- Ensure GCP GDP and GPP compliant documentation
- Finalize SDTM and ADaM deliverables
- Generate SDTM datasets
- Manage clinical trial programming tasks
- Prepare and review annotated CRFs
- Program ADaM
- Provide training on statistical computing environments
- Support clinical study reports
- Support development safety update reports
- Support investigator brochures
- Support periodic safety update reports
- Support risk management plans
Perks/Benefits
Skills/Tech-stack
ADaM | Annotated CRF | Clinical Database | Clinical Practice | Clinical data | Clinical data modeling | Clinical data standards | Data Flow | Data Flow Plan | Data Management | Data Modeling | Data Standards | Define.xml | ECRF | Good Clinical Practice | Good Programming Practice | Good documentation | Good documentation practice | Industry knowledge | Metadata Management | Pharmaceutical Industry | Pharmaceutical industry knowledge | R | SAS | SDTM | Statistical programming | TFL
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
Roles
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