Role : Statistical Programmer
Required skills : SAS, SDTM, ADaM, TLFs
Experience : 3 Plus
Location : Remote
Notice : Immediate to 30 days
Primary Responsibilities
- Communicates effectively with functional leadership concerning project issues (e.g. data, technical, timelines).
- Provides comprehensive programming support for project teams, including development of programming strategies, standards, specifications and programmed analysis. Drives the development and implementation of innovative strategies and technologies to improve programming efficiency.
- Reviews key planning documents (e.g., protocol, statistical analysis plan, mock shells) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements.
- Supports the development of unambiguous and robust programming specifications for programming work.
- Identifies opportunities for increased efficiency and consistency within Inference. Contributes to globalization, improvement and standardization of processes, standards and tools.
Qualification
- 3 - 12 years of experience as a statistical programmer in a clinical environment
- Significant knowledge of SAS software (i.e. Base, Stat, Graph components) and general computing as relates to clinical drug development.
- Graduate degree , certification from SAS preferred. Knowledge of other software (e.g. R) desired.
- Knowledge of the drug development process, clinical trial methodology, statistics and familiarity with global regulatory requirements
- Ability to work successfully within cross-functional teams
- Ability to be flexible and adapt quickly to the changing needs of the organization.
- Ability to organize multiple work assignments and establish priorities.
- Excellent verbal and written communications skills
Suitable Candidates can share the resume to my mail ID [Confidential Information] for an immediate response.
Regards,
Priyadharshini.C
The Whiteboard
