Senior Associate II

Create primary programs to generate deliverables in accordance with TFL shells, programming instructions, and dataset specifications. Validate statistical deliverables to ensure accuracy and compliance. Develop study, project, or global macros to streamline programming processes. Contribute to the development and review of programming dataset specifications. Ensure timely, high-quality, and efficient completion of deliverables. Manage multiple tasks effectively to meet delivery timelines. Identify and resolve programming issues; escalate complex issues as needed. Establish and maintain effective working relationships with study team members. Contribute to the development and improvement of SP standards and processes. Key Requirements / Qualifications: Minimum of 3 years of relevant statistical programming experience in the pharmaceutical or device industry. Demonstrated ability to deliver high-quality and timely SP outputs. Knowledge of internal and external standards and compliance requirements. Ability to work effectively under general supervision and handle multiple tasks. Ensures deliverables meet external quality standards for Health Authorities.