Senior SAS Programmer

Join our innovative team as a Senior SAS Programmer, where you’ll play a critical role in advancing clinical studies within the pharmaceutical industry. We are looking for a highly skilled professional with a robust background in SAS programming, capable of leading programming efforts to produce comprehensive Tables, Listings, and Figures (TLFs).

Your responsibilities

• Take ownership of SAS programming activities, ensuring data analysis aligns with study protocols and statistical analysis plans.
• Develop, test, and maintain SAS programs to produce key trial outputs such as analysis datasets, Tables, Listings, and Figures (TLFs).
• Work closely with cross-functional teams, including statisticians and data managers, to meet project deadlines and ensure high-quality results.
• Lead and guide junior programmers, helping them follow best practices and maintain high programming standards.
• Contribute your expertise to team discussions, offering programming insights during study design and throughout the analysis phase.
• Ensure that all deliverables comply with regulatory requirements and company guidelines.

• Fully remote work – work from anywhere in the EU
• Flexible contract options – COW (Contract of Work) and B2B agreements
• Be a part of high-impact clinical trials that make a difference in healthcare

Benefits

• Internal Mobility Program – enjoy many opportunities for career growth, job rotations, diversity of projects & technologies
• Referral Program – enjoy cooperation with your colleagues and get a bonus!
• 5/10 Years NATEK Club – we offer long-term cooperation and celebrate each fifth-year cooperation anniversary with gifts
• NATEK CSR Events & team buildings – enjoy our values: accountability, partnership and expertise and #workITwithus
• Education – benefit from our know-how, learning courses and certificates and IT events – be part of the community of leaders of the industry and take part as a speaker or a visitor
• Multisport
• Technical and Personal training
• Language courses
• Additionally only for employment contract:
• Cafeteria
• Financial Contribution for Meals
• Life insurance
• Bonuses for Personal Events
• Day off for volunteering

Our requirements

• A degree in Computer Science, Statistics, Mathematics, or a related field (advanced degree is a plus).
• 5+ years of hands-on SAS programming experience within the pharmaceutical, biotechnology, or clinical research sectors.
• Proficiency in SAS/Base, SAS/STAT, SAS/Macro, and relevant SAS modules.
• Strong understanding of CDISC standards (e.g., SDTM, ADaM) for clinical trial data.
• Excellent attention to detail and problem-solving skills, with the ability to work well in a collaborative team environment.
• Previous experience leading programming efforts for clinical trials and mentoring junior programmers is highly desirable.
• Familiarity with regulatory submission processes and guidelines (e.g., FDA, EMA) is advantageous.

Join us and contribute to impactful clinical research efforts that aim to enhance patient outcomes and quality of life!