Statistical Programming Statistical Programmer Consultant - REMOTE Texas
Orbis Clinical is seeking a remote-based Statistical Programmer Consultant for 6 months.
Job Title: Statistical Programmer Consultant
Location: Remote
Contract:6 months
Position Summary:
Working with the Biometrics staff, the Statistical Programmer Consultant provides programming support for Phase 1 to Phase 3 studies, including project integration and disease monitoring project work. Provides timely support to the project team on all statistical programming matters according to the project strategy. Programs SDTM/ADaM/TLFs for the studies, write datasets specification, QC datasets and tables. Identifies and communicates changes in project requirements that may affect key deliverables.
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 1-5 years of clinical trial programming experience in the biotechnology, pharmaceutical or health related industry
- Advanced SAS programming skill s 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 programing projects
- Excellent organizational skills and ability to prioritize tasks
Compensation Details:
- Orbis Clinical is an equal opportunity employer that provides a reasonable range of compensation for our positions. Actual compensation is influenced by a wide array of factors including, but not limited to, skill set, level of experience and specific office location.
- The Pay Range for this position is $81.37 per hour, can vary depending on employment status.
- Orbis Clinical provides W2 Employees with options for Health Benefits and 401K.
EEO and Reasonable Accommodation Statement:
Orbis Clinical provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, housing, age, disability or genetics.
We will consider all qualified applicants for employment, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws.
By applying for this position, you agree that any calls from Orbis Clinical and its subsidiaries may be monitored or recorded for training and quality assurance purposes.