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.

Skills Required
Sas Programming, statistical programming