Statistical Programmer 1 (DM SAS Listings Team)

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Skills you'll use

What you'll do

• 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.

Who can apply

• 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.

About Fortrea

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