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 workplace.
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.
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