Statistical Programmer 1

**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](https://careers.fortrea.com/us/en/eeo-and-accommodations).