R Statistical Programmer

This is a fully remote position, open to applicants in Armenia.

📋 Description

• Utilizes R and SAS to create tailored programming code that generates summary tables, data listings, graphs, and derived datasets as outlined in the statistical analysis plan and programming specifications.

• Ensures that outputs adhere to quality standards and fulfill project requirements.

• Conducts validation programming and collaborates with other programmers, biostatisticians, and project team members to address discrepancies or findings.

• Keeps project team members updated on programming progress and any issues that require their attention.

• Maintains organized, comprehensive, and current project documentation, testing, and verification/quality control documents and programs to ensure readiness for inspection.

• Manages scheduling and time constraints across various projects, establishes goals based on management priorities, and adjusts to changes in timelines or priorities by reorganizing daily tasks.

• Develops specifications for datasets and outputs of varying complexity in accordance with statistical or sponsor requirements.

• Proactively identifies and resolves potential programming issues, demonstrating foresight, establishing a foundation for efficient programming, and accurately defining all variables to ensure acceptance by peer review and sponsors/requestors with minimal rework.

• Conducts effective internal meetings, considering appropriate formats, frequencies, and attendance.

⛳️ Requirements

• Proficiency in R programming is essential.

• Experience with CDISC - SDTM/ADAM programming is required.

• An undergraduate degree, preferably in a scientific or statistical field; alternatively, a combination of education and proven programming experience will be considered.

• Significant programming experience in R or other necessary software, ideally in a clinical trial setting, as evidenced by the ability to lead multiple complex and/or global projects with teams of statistical programmers.

• Familiarity with CDISC Standards for regulatory agency compliance is necessary.

• Experience with submissions to regulatory agencies is preferred.

• Background in mentoring others within the clinical trial process and CDISC Standards.

• Exceptional written and verbal communication skills are required.

• Must be able to read, write, speak, and understand English.

🏝️ Benefits

• We are dedicated to developing our employees through career advancement and progression; supportive and engaged management; technical and therapeutic area training; peer recognition; and a comprehensive total rewards program.

• We are committed to fostering an inclusive culture where you can truly be yourself.