Lead impactful statistical programming projects in a dynamic, remote environment. Collaborate with cross-functional teams to drive clinical trial success. Enhance efficiency and quality through innovative programming solutions.

Statistical Programmer Consultant
in Healthcare + Life Sciences ContractJob Detail
Job Description
Overview
- Collaborate with Biometrics staff to provide programming support for Phase 1 to Phase 3 clinical studies.
- Develop and maintain SDTM/ADaM datasets, TLFs, and dataset specifications for clinical trials.
- Ensure timely and accurate programming deliverables aligned with project strategies and timelines.
- Support project integration and disease monitoring initiatives through statistical programming expertise.
- Identify and address changes in project requirements impacting deliverables.
- Collaborate with cross-functional teams including Clinical Operations, Data Management, and Regulatory staff.
- Contribute to process improvement strategies and identify tools to enhance efficiency and quality.
- Provide technical input for documents developed by biostatisticians, data managers, and medical writers.
Key Responsibilities & Duties
- Perform programming activities across multiple projects and therapeutic areas, internally and externally by CROs.
- Create and review annotated CRFs mapped to SDTM datasets for clinical trials.
- Balance conflicting priorities while promoting communication and alignment with strategic objectives.
- Act as a role model by setting high standards for quality, creativity, and project ownership.
- Develop and maintain data review and reporting tools alongside Biometrics and other functions.
- Provide technical guidance for statistical applications and process improvement strategies.
- Collaborate with cross-functional teams to meet deliverables and timelines for statistical data analysis.
- Identify and implement new tools to improve efficiency and quality in statistical programming.
Job Requirements
- Bachelor’s degree in Statistics, Computer Science, Mathematics, Engineering, or a related discipline required.
- Minimum of 1-5 years of clinical trial programming experience in biotechnology or pharmaceutical industries.
- Proficiency in SAS programming and experience with statistical software such as R and S-Plus.
- In-depth knowledge of CDISC standards, including SDTM, ADaM, and controlled terminologies.
- Strong organizational skills and ability to prioritize tasks effectively.
- Self-directed, technically proficient, and capable of leading statistical programming projects strategically.
- Excellent communication skills for collaborating with cross-functional teams and providing technical input.
- Experience in process improvement and identifying tools to enhance programming efficiency.
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