Statistical Programmer 1 (DM SAS Listings Team)

Job description

**Summary of Responsibilities:** - Provide Statistical Programming support for clinical trial projects. - Develop, validate, and maintain SAS programs and outputs for the management, analysis, and reporting of clinical trial data. - Develop and maintain data transfer programs in accordance with client specifications and project requirements. - Develop Data Management (DM) SAS listings as per client specifications and study standards. - Review draft and final production outputs to ensure quality, accuracy, and consistency. - Take ownership of the quality and integrity of all assigned deliverables. - Collaborate effectively with cross-functional teams, including Clinical Data Management, Statistical Programming, and other project stakeholders. - Effectively prioritize and manage multiple studies, tasks, and competing priorities in a fast-paced environment, consistently delivering high-quality results while meeting project timelines and deliverables. - Demonstrate a positive and professional attitude, contributing to a collaborative and productive team environment. - Continuously develop technical, industry, and project-related knowledge and skills. - Maintain a high level of attention to detail and ensure all work is delivered to the highest quality standards. - Develop strong problem-solving skills and proactively seek guidance from senior Statistical Programming staff when required. - Gain knowledge of broader Statistical Programming activities and responsibilities under the guidance of senior team members. - Adhere to Fortrea Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and Quality Management System (QMS) requirements. - Support process improvement initiatives and contribute to operational excellence within the department. - Perform additional duties and responsibilities as assigned by senior Statistical Programming staff or management. **Qualifications (Minimum Required):** - Bachelor's degree in computer science, Life Sciences, Mathematics, Statistics, or a related discipline. - Fortrea may consider relevant and equivalent experience in lieu of educational requirements. - Language Skills Required: Speaking: English required Writing/Reading: English required **Experience (Minimum Required):** - 1 to 3 years of SAS programming experience in the CRO or Pharmaceutical Industry, or an equivalent combination of education, with a solid understanding of programming fundamentals and program development principles. - Mandatory experience in developing and maintaining vendor data programs. - Experience in coding, database reconciliation, PK deviation analysis, and development of custom listings is advantageous. - Experience in SAS macro development, debugging, and working with complex macros would be an advantage. - SAS certification is desirable but not mandatory. - Understanding of the clinical trial process. - Ability to work effectively with cross-functional teams and stakeholders. - Results-driven with a strong focus on delivery and accountability. - Strong attention to quality and continuous improvement. **Physical Demands/Work Environment:** - Office environment (Hybrid) Learn more about our EEO & Accommodations request here .