Statistical Programmer
3 weeks ago
Job Summary:
NexPro Technologies Inc is seeking a highly skilled Statistical Programmer to join our team. As a Statistical Programmer, you will be responsible for preparing study protocols and reports, conducting statistical analysis on clinical trial data, and generating randomization schedules.
Key Responsibilities:
- Assist the Director of Biostatistics and Data Management in preparing study protocols and reports.
- Conduct statistical analysis on clinical trial data to produce tables, reports, and graphs.
- Generate randomization schedules and provide technical and project management skills in SAS programs.
- Maintain project administration files, including protocols, annotated case report forms, and statistical analysis plans.
- Participate in standard operating procedures, process improvements, system validation, and integration of new tools and technologies.
- Lead approaches to database design using CDISC standards and CDISC/eCTD requirements for regulatory submissions.
- Oversee data integration for clinical summaries and creation and quality control of statistical submission components.
Requirements:
- Master's degree or foreign equivalent degree in Healthcare Informatics, Health Admin, Pharmacology, Toxicology, Pharmacy, Chemistry, Computer Science, Public Health, Bioinformatics, Biotechnology, Statistics, or related field.
- Strong knowledge of SAS programming and statistical analysis.
- Excellent communication and project management skills.
- Ability to work in a team environment and lead projects.
Benefits:
- Medical, Life Insurance, and 401K.
- Standard Company Benefits.
Travel Requirements:
Position requires travel/relocation to various unanticipated client locations throughout the U.S. with expenses paid by the employer.
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