Job Description

We are seeking a skilled and detail-oriented Clinical SAS Programmer to join our clinical research team. The Clinical SAS Programmer will play a key role in analyzing and reporting clinical trial data using SAS software. The ideal candidate will have a strong background in SAS programming, clinical data management, and a thorough understanding of regulatory requirements in the pharmaceutical or healthcare industry. Responsibilities: Collaborate with cross-functional teams, including biostatisticians, data managers, and clinical research associates, to develop programming specifications and data analysis plans. Design and develop SAS programs to generate tables, listings, and graphs (TLGs) for clinical study reports, regulatory submissions, and other study-related documents. Perform data validation and quality control checks to ensure accuracy and integrity of clinical trial data. Create and maintain SAS datasets, including data transformation, cleaning, and integration from multiple sources. Develop and validate SAS macros and utilities to automate repetitive tasks and improve programming efficiency. Ensure compliance with regulatory guidelines, industry standards, and company SOPs in programming and data handling. Collaborate with statisticians to provide input on statistical analysis plans and assist with statistical programming tasks as needed. Conduct ad-hoc data analyses and generate reports in response to internal and external requests. Participate in data review meetings and provide support for data-related queries from internal and external stakeholders. Stay updated on emerging trends, new methodologies, and advancements in SAS programming techniques. Document programming processes, datasets, and programming specifications in accordance with company standards. Contribute to process improvement initiatives and share best practices within the programming team. Qualifications and Skills: Bachelor s or Master s degree in a relevant scientific discipline (e.g., statistics, biostatistics, computer science). Minimum of 3 years of experience as a Clinical SAS Programmer in the pharmaceutical, biotech, or clinical research industry. Proficiency in SAS programming, including SAS/Base, SAS/STAT, SAS/Graph, and SAS/Macro. Strong understanding of clinical trial data structures, CDISC standards (SDTM and ADaM), and regulatory guidelines (e.g., ICH-GCP). Experience in generating TLGs, tables, and figures for clinical study reports and regulatory submissions. Solid knowledge of data management principles and processes. Familiarity with data visualization tools and techniques. Excellent problem-solving and analytical skills. Detail-oriented with the ability to work on multiple projects and meet deadlines. Good communication and interpersonal skills to collaborate effectively with cross-functional teams. Knowledge of programming languages such as Python or R is a plus. Certification in SAS programming or clinical data management is desirable. Salary and Benefits: Competitive salary based on qualifications and experience. Professional development opportunities to enhance SAS programming skills and knowledge.

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