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TITLE: - Principal Statistical Programmer (Contractor)
REPORTING RELATIONSHIP: - Director, Statistical Programming
SCOPE: - If you want to have an impact on the lives of patients with cancer, take a look at Client With our diverse pipeline, passionate team, and extensive resources, we offer abundant opportunities to contribute to the transformation of cancer care.
- We know that every team member, regardless of their role, plays a critical part in advancing research and making a difference in the lives of patients with cancer.
KEY RESPONSIBILITIES: - Lead on clinical studies and integrated analyses and provide guidance and training to other lower level personnel.
- Develop or evaluate software tools, SAS macros, utilities to automate programming activities and support Biometrics team collaboration.
- Contribute and implement to statistical analysis plans; provide additional expertise in the analysis of clinical trial when it relates to protocol development, case report form design and data collection.
- Review Data Management Plan, Data Transfer Plan, Data Validation Plan and Edit Check Specifications and provide comments.
- Work closely with Biostatistics to create analysis specifications following the instructions provided in Statistical Analysis Plan (SAP).
- Create CDISC SDTM and ADaM files, SAS export files, Define.xml and Reviewer's Guide for Electronic Submission.
- Perform Data analysis, statistical analysis, generate safety and efficacy tables, listings and graphs using Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL and SAS/ODS.
- Interact with Statisticians and other clinical team, perform ad hoc analysis and generate outputs according to the requirements.
- Help identify issues and initiates resolution of the problems.
- Act as a liaison between statistical programming, subcommittees and project teams as needed.
- May serve as external spokesperson for the organization.
- Create/acquire tools to improve programming efficiency or quality control.
- Stay current with industry trend, best practices and improves statistical programming methodology.
- Other duties as assigned.
PROFESSIONAL EXPERIENCE / QUALIFICATIONS: - Minimum 10 years Pharmaceutical/Biotech programming experience including macro/tools development experience.
- FDA submission experience is highly desirable.
- Strong SAS programming and Statistical background with strong skills in SAS Base, SAS/Macros, SAS/Graph and SAS/Stat.
- Ability to use professional concepts to achieve objectives in creative and effective ways.
- Experienced in managing multiple projects.
- Solid knowledge of SAS Programming language, Software Development Life Cycle and CDISC standards (SDTM & ADaM).
- Solid knowledge of other software such as R etc. is a plus.
- BS/MS in Statistics, Math or Scientific Discipline.
Skills: Required: - PHARMACEUTICAL/BIOTECHSASSTATISTICSBIOMETRICS
Additional: - STATISTICAL PROGRAMMING
- FORM DESIGN
- MARKETING ANALYSIS
- STATISTICAL ANALYSIS
- ODS
- CASE REPORT
- QUALITY CONTROL
- DATA VALIDATION
- BIOSTATISTICS
- LIAISON
- CLINICAL TRIALS
- ERIAL ATTACHED SCSIDATA MANAGEMENT
- OPERATIONAL DATA STORE
- SQL
- XML
- DATA ANALYSIS
- COLLECTION
- FDA
- AD HOC ANALYSIS
- SAPCLINICAL STUDIES
Date Posted: 24 March 2025
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