
Senior Statistical Programmer
Posted 6 days ago

Posted 6 days ago
This is a fully remote position, open to applicants in China.
• Utilize SAS or alternative software to create customized programming code for summary tables, data listings, graphs, and derived datasets in line with statistical analysis plans and programming specifications.
• Ensure that outputs adhere to quality benchmarks and project stipulations.
• Conduct validation programming and address discrepancies in collaboration with Programmers, Biostatisticians, and project team members.
• Keep team members updated on programming advancements and challenges.
• Comply with relevant SOPs, WIs, and regulatory requirements such as ICH.
• Maintain thorough, organized, and current project documentation, testing, verification, and quality-control materials to ensure inspection readiness.
• Manage timelines and constraints across various projects while adjusting workload according to shifting priorities.
• Create specifications for datasets and outputs of varying complexities.
• Identify and mitigate programming challenges and define variables for peer reviews and sponsor/requestor approvals.
• Prepare for and lead productive internal meetings, disseminate information and minutes, and ensure follow-through on action items.
• Negotiate time estimates and complete study programming tasks within designated timeframes.
• Serve as the lead statistical programmer and oversee the programming activities of other programming staff.
• Review Statistical Analysis Plans, mock shells, programming specifications, annotated CRFs, and SAS database designs.
• Participate in sponsor, kickoff, and bid defense meetings as the statistical programming representative.
• Mentor programming staff through training, work reviews, feedback, and guidance.
• Transfer deliverables and carry out other assigned work-related responsibilities.
• Bachelor’s degree, ideally in a scientific or statistical field; an equivalent combination of education and relevant programming experience may be considered in lieu of a degree.
• Significant programming experience in SAS or other necessary software, preferably within a clinical trial context.
• Outstanding written and verbal communication abilities.
• Proficient in reading, writing, speaking, and understanding English.
• Opportunities for career development and advancement.
• Supportive and engaged line management.
• Technical and therapeutic area training.
• Peer recognition and total rewards program.
• An inclusive culture.
• Comprehensive resources, including emerging technologies, data, science, and knowledge sharing.
• Minimal travel may be required.
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