Senior/Principal Statistical Programmer - UK (Remote or Office Based)

Veramed; Leigh on Sea; Hybrid; GBP 40,000 - 80,000; Full time

Job summary

An innovative firm is seeking a Senior/Principal Statistical Programmer to deliver impactful programming solutions in a flexible environment. This role involves programming and quality control of datasets, developing specifications aligned with industry standards, and mentoring junior staff. You will work collaboratively with top pharma clients, ensuring timely and high-quality deliverables. With opportunities for growth and exposure to diverse projects, this position is perfect for those passionate about quality and making a difference in the field of clinical development.

Benefits

Flexible Work Options

Training Opportunities

Competitive Salary Package

Qualifications

• Experience in statistical programming and quality control of datasets.
• Knowledge of ICH and CDISC standards.

Responsibilities

• Program and QC datasets following specifications and best practices.
• Mentor junior staff and lead programming roles across therapeutic areas.

Skills

SAS

R

Time Management

Clinical Drug Development Knowledge

Job description

Senior/Principal Statistical Programmer - UK (Remote or Office Based)

This role is with Veramed, focusing on delivering high-impact programming solutions in an FSP-style environment. The company emphasizes providing exceptional statistical and programming consultancy while fostering a supportive workplace that promotes personal and professional growth.

Key Responsibilities:

• Program and QC datasets and TFLs following specifications and best practices.
• Develop dataset specifications aligned with CDISC standards.
• Participate in study team meetings and mentor junior staff.
• Communicate with study team members and clients, ensuring timely, high-quality deliverables.
• Lead programming or technical roles across various therapeutic areas and phases.
• Present at industry conferences and contribute to innovative study reporting solutions.

What to Expect:

• A collaborative environment supporting growth and development.
• Exposure to diverse projects and top pharma clients.
• Ownership of your role with opportunities to expand skills.

Beneficial Experience:

• Knowledge of clinical drug development and relevant standards (ICH, CDISC).
• Proficiency in SAS or R, depending on experience.
• Strong time management and ability to work independently and in teams.

If you are passionate about quality and mentoring, and want to make an impact, apply now! We offer flexible work options, training, and a competitive package.

Veramed values diversity and is an equal opportunities employer, committed to a respectful and inclusive workplace.