Statistical Programming Team Lead
3 days ago
Clinovo is a leading provider of clinical research professionals, empowering healthcare and life science companies to succeed. We are seeking an experienced Associate Principal Statistical Programmer to join our team.
About the RoleThis is a challenging opportunity for a skilled statistical programmer to lead programming activities at the study or project level. You will use your expertise in SAS software to create and maintain macros, listings, tabulations, graphical summaries, and formal statistical estimates and tests. Additionally, you will be responsible for creating datasets in standard format (SDTM), analysis datasets, and assessing the quality of data analysis programs.
Key Responsibilities- Maintain existing macros, provide training on macro usage, develop documentation and training materials, and serve as the point of contact for macro questions.
- Follow the Software Development Lifecycle (SDLC) to create new global macros and standard programs that meet department needs.
- Develop SAS or other programs, and specifications, for use in study or other analyses, such as Integrated Safety Summaries.
- Work with clinical data management staff and biostatisticians to coordinate and schedule data transfers and the delivery of required outputs.
- A BS/BA degree in a related discipline and a minimum of eleven years of related experience; or a MS/MA degree in a related discipline and a minimum of nine years of related experience; or a PhD in a related discipline and a minimum of five years of related experience.
- At least eight years' experience in Pharmaceutical/Biotech programming.
- Demonstrated proficiency in SAS/Base, SAS/Stat, and SAS/Macros.
The base salary compensation for this role is MID range: $154,500 - $219,500 annually. Clinovo is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind.
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