R&D Programmer III, Poland

Krakow, Malopolskie N/A PL

Posted: 10/08/2025 2025-10-08 2025-11-09 Employment Type: Contract Job Category: Statistical Programming Job Number: 622983 Is job remote?: Yes Country: Poland

Job Description

We’re currently recruiting for a Statistical Programming Contractor on behalf of a global biopharmaceutical company.

This is a senior-level contract role ideal for an experienced SAS programmer with a strong background in clinical trials and CDISC standards. If you’re looking for a high-impact opportunity to contribute to global studies and publications, we’d love to hear from you.

About the Role

As a Statistical Programming Contractor, you’ll provide comprehensive programming support across clinical trial projects, including development of analysis datasets, tables, listings, and graphs (TLGs). You’ll work independently on global assignments, support regulatory submissions, and contribute to publications for marketed drugs.

This role is fully remote with no travel required.

Key Responsibilities

• Lead programming activities at the study and program level
• Develop ADaM specifications, analysis datasets, and TLGs in compliance with regulatory standards
• Support CDISC-based e-submissions and quality control processes
• Standardize deliverables across studies and therapeutic areas
• Collaborate with cross-functional teams and proactively communicate project status
• Provide input on process improvements and programming standards
• Support publication programming for marketed products

What We’re Looking For

Required:

• Bachelor’s degree + 7 years or Master’s degree + 6 years in pharmaceutical or clinical research programming
• Strong knowledge of clinical trials, drug development, and statistical concepts
• Expertise in SDTM and ADaM standards
• Advanced SAS programming skills and experience with tools like Pinnacle 21 and XML
• Ability to work independently and manage global tasks

Preferred:

• Experience with Bioresearch Monitoring (BIMO) deliverables and ISS/ISE datasets
• Solid understanding of statistical models for efficacy analysis
• Familiarity with regulatory frameworks (CDISC, ICH)
• Key Competencies
• Problem-solving and decision-making in complex programming scenarios
• Clear and professional communication skills (written and verbal)
• Ability to influence and collaborate across teams
• Strong organizational skills and attention to detail
• Commitment to continuous improvement and quality delivery

This is an excellent opportunity for a seasoned contractor to contribute to high-profile clinical programs in a flexible, remote setting.

Equal Opportunity Employer: We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.

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