4680 IT & Software Developer jobs in the US
Requirements
Must:
- Bachelors Degree in a technical or scientific field
- 2+ years of SAS programming experience with at least 1 year in a clinical setting
- Proven SAS report programming abilities and an aptitude for independently handling in-house SAS requests
- Familiarity with AI-enabled tools (e.g., AI-assisted coding, data exploration, documentation) and a readiness to embrace new analytical technologies
- Strong foundational programming skills and the capacity to learn and employ additional languages, tools, or platforms as necessary
- Working knowledge of statistical methods commonly utilized in clinical trials and support for biostatisticians in data analysis
- Understanding of data processing, database design, and organization within a clinical data environment
- Basic familiarity with Food and Drug Administration (FDA) regulations and Standard Operating Procedures (SOP) relevant to clinical studies
Responsibilities
- Execute SAS programming to support clinical trials, generating data tables, listings, and reports
- Independently validate statistical programming outcomes
- Assist in drafting statistical analysis plans and contribute to the statistical sections of clinical trial protocols
- Extract real-world evidence from diverse data sources to support ongoing clinical research projects
- Ensure prompt delivery of requested tables, listings, and summaries for users utilizing SAS
- Develop SAS programs for creating clinical insights from real-world data sources such as national registries and commercial datasets
- Periodically assess and report on data trends and integrity, conducting meta-analyses across studies to meet business requirements
- Provide programming and statistical analysis support for FDA submissions, post-marketing reports, EU MDR submissions, ODEP ratings, and professional journal publications
- Collaborate with biostatisticians for complex analyses to bolster publications and reports
- Review and contribute to statistical analysis plans for Investigational Device Exemption (IDE) clinical studies and other real-world trials
- Produce study reports using RAVE reporting functions, BO4, and SAS/R
- Validate study summary reports employing SAS or R
- Engage in ongoing improvement initiatives and process reengineering projects in support of our clinical efforts
Description
We are excited to announce an opportunity to join our Joint Replacement Division as a Senior SAS Programmer, Clinical Data Scientist. This hybrid role is based in Mahwah, New Jersey, requiring onsite presence two to three days each week. We offer competitive compensation between $100,000 and $166,600, along with bonus eligibility and comprehensive benefits. As a valued member of our team, you will play a crucial role in supporting clinical trials and contributing to significant research initiatives.
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The company with most openings is Judge Group, Inc. as they are hiring for 362 different DevOps jobs in the United States. They are probably quite committed to find good DevOps.