Senior & Principal Statistical Programmers

R&D Partners; Leeds; On-site; GBP 50,000 - 70,000; Full time

Job summary

A specialized clinical research organization in Leeds is looking for Senior and Principal Statistical Programmers to lead the design and validation of SAS programs for clinical trials. The ideal candidate must have the right to work in the UK/EU and experience in statistical programming within pharma or related fields. This role involves collaborating with biostatisticians, performing quality checks, and mentoring junior programmers. The company emphasizes growth and innovation in statistical programming.

Qualifications

• Full right to work in UK / EU.
• Experience in Statistical Programming within Pharma, Biotech, CRO, Medical Device, or similar company.
• Skilled communicator to Statistical Programming and Non-Statistical Programming personnel.

Responsibilities

• Lead/support SAS program design and validation for clinical trial data.
• Collaborate with biostatisticians on analysis plans and statistical methods.
• Perform QC checks on statistical outputs for project compliance.
• Assist in statistical report preparation and regulatory submissions.
• Mentor junior programmers and share best practices.

Skills

Statistical Programming

Communication

Job description

Lead the code behind clinical breakthroughs-join a CRO investing in the future of Statistical Programming.

R&D Partners is seeking Senior and Principal Statistical Programmers to join a highly specialized CRO that is investing heavily in the growth of its Statistical Programming function.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities :

• Lead / support the design, development and validation of SAS programs for statistical analysis and reporting of clinical trial data
• Collaborate closely with biostatisticians to create comprehensive analysis plans and apply appropriate statistical methods.
• Perform QC checks and review statistical outputs to ensure compliance with project specifications and regulatory guidelines.
• Assist in the preparation of statistical reports, presentations, and regulatory submissions to support clinical development programs.
• Mentor junior programmers and contribute to team development by sharing best practices and technical knowledge.

Key Skills and Requirements :

• Full right to work in UK / EU
• Experience in Statistical Programming within a Pharma, Biotech, CRO, Medical Device or similar company
• Skilled communicator to Statistical Programming and Non-Statistical Programming personnel

For more information, please contact George Breen.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

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