
Senior Statistical Programmer, SAS Programmer
Posted 3 days ago

Posted 3 days ago
This is a fully remote position, open to applicants in Poland, +2 more countries.
• Develop SAS programs to create derived analysis datasets and produce content for tables, listings, and figures.
• Conduct programming validation to ensure the accuracy of analysis datasets and programming outputs.
• Offer programming support to project teams.
• Formulate programming strategies, standards, specifications, and programmed analyses.
• Assist in the preparation and review of electronic submissions.
• Evaluate statistical analysis plans, data presentation plans, and data review plans for consistency and programming assumptions.
• Analyze the impact of planning documents on programming tasks.
• Collaborate with vendors concerning project standards, programming conventions, specifications, and file transfers.
• Ensure the quality of deliverables by adhering to standards and complying with regulatory requirements, guidance, SOPs, and work practices.
• Identify opportunities for enhancing efficiency and consistency within the team and with vendor interactions.
• Independently manage and/or execute programming tasks with minimal oversight.
• Contribute to improvement initiatives.
• A Bachelor’s degree in statistics, biostatistics, mathematics, computer science, or life sciences is required.
• Expertise in SAS is essential.
• Several years of experience in clinical/statistical programming within pharmaceutical clinical development.
• Proven proficiency in analytical programming.
• Comprehensive understanding of clinical data structures, including CDISC standards, and relational databases.
• Demonstrated skills in using MS Office, XML, and Pinnacle 21.
• Proven ability to manage and process upstream data, including various data forms, workflow, eDC, and SDTM.
• Proven ability to generate outputs that meet downstream requirements, including ADaM, Data Definition Table, and e-submission.
• Strong understanding of regulatory, industry, and technological standards and requirements.
• Good knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs.
• Proven ability to collaborate effectively in a team environment with clinical team members.
• Exceptional long-term job stability and growth opportunities.
• Flexibility to maintain your personal life.
• A welcoming and friendly workplace atmosphere.
• Opportunities for long-term career development.
• Chance to grow within the role and take on additional responsibilities or enhance skills in related departments.
• Fully flexible work arrangements; entirely home-based options available.
• Office desk provided for employees residing nearby who wish to utilize it.
• Incentive plans, bonuses, and/or additional forms of compensation may be available based on the position.
• Health, welfare, and various employee benefits offered.
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