Statistical Programmer II – FSP

This is a fully remote position, open to applicants in Poland, +3 more countries.

📋 Description

• Offer technical expertise for the execution of clinical trials.

• Assist in programming tasks connected to the analysis and reporting of clinical study data with minimal oversight.

• May assume the role of Statistical Programming Lead, or part of it, for small, uncomplicated projects.

• Provide high-quality service utilizing client systems and adhering to client processes.

• Collaborate closely with client teams and Parexel colleagues in a global context.

• Generate derived datasets, including SDTM and ADaM, as well as tables, figures, and data listings of varying complexity.

• Conduct quality control on low to medium complexity derived datasets, tables, figures, and data listings.

• Create and review specifications for derived datasets and other supporting documents.

• Ensure complete traceability and regulatory compliance.

• Engage in and contribute to knowledge-sharing sessions within the programming community.

⛳️ Requirements

• Bachelor’s degree in statistics, biostatistics, mathematics, computer science, or life sciences.

• At least 3 years of SAS programming experience in clinical research.

• Proficiency in SAS Base, SAS/STAT, SAS/GRAPH, and SAS macros.

• Strong knowledge of CDISC standards.

• Familiarity with statistical terminology, clinical tests, and protocol designs.

• Exceptional attention to detail with a focus on quality.

• Excellent written and verbal communication skills in English.

🏝️ Benefits

• Fully flexible work arrangement; the possibility to work entirely from home.

• A welcoming and friendly work atmosphere.

• Opportunities for long-term career development.

• Potential for growth within the role and the chance to take on additional responsibilities.

• Opportunities to enhance skill sets across other related departments.

• Long-term job security and future prospects.