SAS Programmer

Solutions Delivery - Kosice, Frankfurt

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About Arcondis

Arcondis is a global consulting company with an exclusive focus on the healthcare and life science industries, with their particularly demanding requirements on quality and regulatory aspects. We have been managing challenges and solving problems for our clients in the areas of compliance, business processes,

information technology, and digital transformation since 2001. We create value through cross-functional, sophisticated delivery methodologies and intelligent implementation. Our clients love to work with us because of our unique skillsets, our pragmatic approach, and our will to win.

About us
Open Position
Mission

Tasks and responsibilities

  • Create, revise, and review SDTM mapping specifications for mapping purposes.

  • Collaborate with the Technical Services team to implement mapping strategies.

  • Develop and maintain SAS programs to support data analysis and reporting needs.

  • Perform data cleaning, validation, and quality control procedures.

  • Generate tables, listings, and figures for clinical study reports.

  • Collaborate with cross-functional teams to ensure data integrity and accuracy.

  • Stay updated with industry standards and best practices in SAS programming.

  • Provide technical support and guidance to team members as needed.

  • Participate in the development and improvement of programming processes and standards.

Studies

Your profile

  • Bachelor's degree in Computer Science, Statistics, or a related field.

  • Proven experience as a SAS Programmer in a professional setting.

  • Strong proficiency in SAS programming language and SAS macro language.

  • Familiarity with CDISC standards and SDTM mapping specifications.

  • Experience working with Technical Services or similar departments is preferred.

  • Excellent problem-solving and analytical skills.

  • Attention to detail and ability to work with large datasets.

  • Strong communication and interpersonal skills.

  • Ability to work independently and collaboratively in a team environment.

  • Familiarity with clinical research and regulatory requirements is a plus.

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