Statistical Programmer 1 DM SAS Listings Team

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)

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