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Senior SAS Programmer

Remote:

Full Remote

Contract:

Freelance

Experience:

Senior (5-10 years)

Work from:

United States

Offer summary

Qualifications:

Degree in Computer Science or related field, 5+ years of SAS programming experience, Proficiency in SAS/Base, SAS/STAT, SAS/Macro, Strong understanding of CDISC standards, Experience with regulatory submission processes.

Key responsabilities:

Take ownership of SAS programming activities
Develop and maintain SAS programs for trial outputs
Collaborate with cross-functional teams
Lead and mentor junior programmers
Ensure compliance with regulatory requirements

NATEK Information Technology & Services SME https://natek.eu/

501 - 1000 Employees

See more NATEK offers

Job description

Job Description

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).

What We Offer:

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

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.

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!

Benefits

For all contacts:

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

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