Principle Statistical Programmer
Principle Statistical Programmer
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Salary Not Disclosed
1 Vacancy
Job Description
Responsibilities:
- Provide quality deliverables by following corporate and departmental policies procedures and applicable standards.
- Perform data manipulation analysis and reporting of clinical trial data.
- Create analysis files tables listings and figures and validation of those files.
- Maintain project tracking and validation documentation.
- Work well in an environment where team members may be distributed across multiple locations.
- to ensure project objective alignment clarity accuracy and completeness of programming requirements.
- Present statistical programming concepts to nonprogramming team members as necessary.
- Collaborate effectively with crossfunctional teams and interface with multiple stakeholders to manage timelines and priorities.
- Serve as backup to Principle Statistical Programmer as needed.
Requirements:
- 710 years statistical programming experience with pharmaceutical/ CRO industry is required.
- Strong Macro Development experience is required.
- PK/PD Programming is a big plus.
- Review planning documents (Statistical Analysis Plan dataset specifications etc..
- Required Qualifications BA/BSc or Masters in Statistics Mathematics Computer Science Life Sciences or other related scientific subject with 78 years of relevant experience.
- Extensive regulatory submission and response experience.
- In depth SAS Programming background with excellent analysis and reporting skills.
- Command of drug development life cycle and experience with the manipulation analysis and reporting of clinical trials data.
- Thorough knowledge of latest CDISC SDTM ADaM and Define standards.
- Ability to effectively oversee geographically diverse programming teams.
- Project management or project planning experience on small to large scale drug development projects.
- In depth knowledge of SAS Graph and Stat packages.
Employment Type
Full Time
