Statistical Programmer Position Available In Mecklenburg, North Carolina
Tallo's Job Summary: Statistical Programmer position at Katalyst Healthcares & Life Sciences in Charlotte, NC. Contract role with an estimated salary of $107K - $126K a year. Responsibilities include programming activities on multiple projects/studies, creating annotated CRF to SDTM datasets, and providing technical input for document production. Requirements include a Master's Degree, 5 years of clinical trial programming experience, and proficiency in SAS, R, and CDISC standards.
Job Description
Statistical Programmer Katalyst Healthcares & Life Sciences – 4.0
Charlotte, NC Job Details Contract Estimated:
$107K – $126K a year 23 hours ago Qualifications Statistical software Biotechnology Statistics Computer Science SAS 5 years R Master’s degree CDISC standards Organizational skills Clinical trials Senior level
Full Job Description Responsibilities:
Involved in the programming activities on multiple projects/ studies across various therapeutic areas, both internally and externally by CROs. Creates and reviews annotated CRF to SDTM datasets. Provides support in balancing conflicting priorities, promoting communication and adequate information flow to motivate, encourage and align people with the company’ s strategic objectives. Functions as a positive role model for setting high expectations for quality, creativity and project ownership. Works collaboratively with Clinical Operations, Clinical Data Management, Global Drug Safety, Regulatory and Project Management management/staff to meet project deliverables and timelines for statistical data analysis and reporting. Provides technical input into documents produced by other functions (e.g., biostatisticians, data managers, medical writers). Works with Biometrics and other functions for the development and maintenance of the data review and reporting tools, and any other statistical applications as appropriate. Involved with the strategy for process improvement. Identifies new tools to increase efficiency and quality.
Requirements:
Master’s Degree in Statistics, Computer Science, Mathematics, Engineering or related discipline. Minimum of 5 years of clinical trial programming experience in the biotechnology, pharmaceutical or health related industry. Advanced SAS programming skills and experience in other statistical software, such as R and S-Plus. Experience and in-depth knowledge in CDISC including SDTM, ADaM, and controlled terminologies. Self-directed, technically strong, and a recognized leader maintaining a strategic prospective with regards to statistical programming processes, management of statistical programming projects. Excellent organizational skills and ability to prioritize tasks.
