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Principal Statistical Programmer

AL Solutions

United Kingdom

Remote

GBP 50,000 - 90,000

Full time

10 days ago

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Job summary

Join a forward-thinking company as a Principal Statistical Programmer and lead innovative statistical programming efforts. This remote position offers the chance to work with a dynamic global team, focusing on complex interventional studies and ensuring compliance with regulatory standards. You'll mentor junior programmers, develop SAS programs, and act as the primary contact for clients. With clear progression paths and a commitment to investing in talent, this role is perfect for those passionate about clinical research and ready to make a significant impact in the biopharmaceutical industry.

Benefits

Competitive Salary

Comprehensive Benefits Package

Leadership Opportunities

Dynamic Global Team Environment

Qualifications

8+ years of experience as a Statistical Programmer in CRO, Biotech, or Pharma.
Proven expertise in SAS programming and CDISC standards.

Responsibilities

Lead statistical programming activities across multiple studies.
Develop and validate SAS programs for clinical trials.

Skills

SAS Programming

CDISC Standards

Statistical Analysis

Leadership Skills

Problem-Solving

Communication Skills

Education

Bachelor's Degree in a Scientific Discipline

Master's Degree in a Related Discipline

Tools

SAS

6 days ago Be among the first 25 applicants

Direct message the job poster from AL Solutions

Expert in linking Biometrics, Biologics and CMC Professionals to Biotech and CDMOs throughout the United States and Canada.

Position: Principal Statistical Programmer

Location: Remote, UK

Are you an experienced Statistical Programmer looking to take the next step in your career? Join a leading, award-winning global CRO that partners with top biopharmaceutical companies to drive innovative clinical research across multiple therapeutic areas.

George Higginson and his team are seeking a Principal Statistical Programmer to provide leadership and technical expertise on complex interventional studies and programs. This is a remote-based role open to candidates across the UK.

Main Responsibilities:

Lead statistical programming activities across multiple studies or an entire program.
Develop and validate SAS programs for the creation of SDTM, ADaM datasets, and TLFs (tables, listings, figures).
Ensure compliance with CDISC standards and regulatory requirements.
Mentor and support junior programmers and contribute to departmental process improvement initiatives.
Act as the primary programming contact for clients and internal project teams.

Requirements:

Over 8 years of experience as a Statistical Programmer within a CRO, Biotech or Pharma.
Bachelor’s or Master’s degree in a scientific, statistical, or related discipline.
Extensive experience with SAS programming in a clinical trial environment.
Proven expertise in CDISC standards (SDTM, ADaM) and regulatory submission processes.
Strong leadership, problem-solving, and communication skills.
Previous experience within a CRO environment is highly desirable.

What’s On Offer:

Opportunity to work with a dynamic and collaborative global team.
Clear progression paths and leadership opportunities.
Competitive salary and comprehensive benefits package.

Join a company that truly invests in its people, technology, and clients. If you’re passionate about clinical research and ready to lead from the front, we’d love to hear from you.

Apply today to take the next step in your leadership journey!

Seniority level

Seniority level
Mid-Senior level

Employment type

Employment type
Full-time

Job function

Job function
Research, Science, and Analyst
Industries
Staffing and Recruiting, Pharmaceutical Manufacturing, and Research Services

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